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2783-17-7

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2783-17-7 Usage

Chemical Properties

WHITE CRYSTALLINE SOLID

Uses

Different sources of media describe the Uses of 2783-17-7 differently. You can refer to the following data:
1. Feedstock for polymer synthesis. Source of twelve carbon chain for medicinal drugs.1
2. 1,12-Diaminododecane is used for synthesis of medicinal drugs, polymers.

Definition

ChEBI: An alkane-alpha,omega-diamine that is dodecane substituted by amino groups at positions 1 and 12.

Flammability and Explosibility

Notclassified

Check Digit Verification of cas no

The CAS Registry Mumber 2783-17-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,7,8 and 3 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 2783-17:
(6*2)+(5*7)+(4*8)+(3*3)+(2*1)+(1*7)=97
97 % 10 = 7
So 2783-17-7 is a valid CAS Registry Number.
InChI:InChI=1/C12H28N2/c1-2-3-4-5-6-7-8-9-10-11-12(13)14/h12H,2-11,13-14H2,1H3

2783-17-7 Well-known Company Product Price

  • Brand
  • (Code)Product description
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  • Detail
  • Alfa Aesar

  • (L04258)  1,12-Diaminododecane, 98+%   

  • 2783-17-7

  • 5g

  • 260.0CNY

  • Detail
  • Alfa Aesar

  • (L04258)  1,12-Diaminododecane, 98+%   

  • 2783-17-7

  • 25g

  • 738.0CNY

  • Detail
  • Aldrich

  • (D16401)  1,12-Diaminododecane  98%

  • 2783-17-7

  • D16401-5G

  • 329.94CNY

  • Detail
  • Aldrich

  • (D16401)  1,12-Diaminododecane  98%

  • 2783-17-7

  • D16401-25G

  • 859.95CNY

  • Detail

2783-17-7SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name dodecane-1,12-diamine

1.2 Other means of identification

Product number -
Other names 1,12-dodecadiamine

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:2783-17-7 SDS

2783-17-7Synthetic route

1,12-dodecanedinitrile
4543-66-2

1,12-dodecanedinitrile

1,12-Diaminododecane
2783-17-7

1,12-Diaminododecane

Conditions
ConditionsYield
With hydrogen; sodium methylate In methanol at 130℃; under 37503.8 Torr; for 5h;91.7%
With lithium aluminium tetrahydride
With triisobutylaluminum
1,12-diazido-dodecane
113665-32-0

1,12-diazido-dodecane

1,12-Diaminododecane
2783-17-7

1,12-Diaminododecane

Conditions
ConditionsYield
With cerium(III) chloride; sodium iodide In acetonitrile for 24h; Heating;55%
With trimethylphosphane In water-d2 at 20℃; for 25h; Staudinger Azide Reduction;
2C36H60O30*C12H28N2

2C36H60O30*C12H28N2

A

1,12-Diaminododecane
2783-17-7

1,12-Diaminododecane

B

C36H60O30*C12H28N2

C36H60O30*C12H28N2

Conditions
ConditionsYield
In water-d2 at 24.85℃; pH=7.3; Equilibrium constant; Decomposition;
C36H60O30*C12H28N2

C36H60O30*C12H28N2

A

1,12-Diaminododecane
2783-17-7

1,12-Diaminododecane

B

alpha cyclodextrin
10016-20-3

alpha cyclodextrin

Conditions
ConditionsYield
In water-d2 at 24.85℃; pH=7.3; Equilibrium constant; Decomposition;
decamethylene-dicarboxylic acid dinitrile

decamethylene-dicarboxylic acid dinitrile

1,12-Diaminododecane
2783-17-7

1,12-Diaminododecane

Conditions
ConditionsYield
With ethanol; sodium
dodecamethylene-diphthalimide

dodecamethylene-diphthalimide

1,12-Diaminododecane
2783-17-7

1,12-Diaminododecane

Conditions
ConditionsYield
With hydrogenchloride
chloroform
67-66-3

chloroform

dodecane-dicarboxylic acid-(1.12)

dodecane-dicarboxylic acid-(1.12)

1,12-Diaminododecane
2783-17-7

1,12-Diaminododecane

Conditions
ConditionsYield
With tris-(2-chloro-ethyl)-amine; sulfuric acid at 35 - 45℃;
ethanol
64-17-5

ethanol

1,12-dodecanedinitrile
4543-66-2

1,12-dodecanedinitrile

sodium

sodium

1,12-Diaminododecane
2783-17-7

1,12-Diaminododecane

1,10-dichlorodecane
2162-98-3

1,10-dichlorodecane

1,12-Diaminododecane
2783-17-7

1,12-Diaminododecane

Conditions
ConditionsYield
Multi-step reaction with 2 steps
1: dimethylformamide
2: H2, NH3 / Raney-Ni / methanol
View Scheme
6-chlorohexanoic acid
4224-62-8

6-chlorohexanoic acid

1,12-Diaminododecane
2783-17-7

1,12-Diaminododecane

Conditions
ConditionsYield
Multi-step reaction with 3 steps
1: Na / methanol / (electrolysis)
2: dimethylformamide
3: H2, NH3 / Raney-Ni / methanol
View Scheme
dodecanedial
38279-34-4

dodecanedial

1,12-Diaminododecane
2783-17-7

1,12-Diaminododecane

(1E,5E,9Z)-cyclododeca-1,5,9-triene
706-31-0

(1E,5E,9Z)-cyclododeca-1,5,9-triene

1,12-Diaminododecane
2783-17-7

1,12-Diaminododecane

Conditions
ConditionsYield
Multi-step reaction with 3 steps
1.1: ozone / acetic acid methyl ester / 1.5 h / 5 °C
1.2: 15 - 20 °C
2.1: 5%-palladium/activated carbon; hydrogen / acetic acid methyl ester; water / 5.5 h / 15 - 25 °C / 11103.3 Torr / Autoclave
3.1: ammonium hydroxide / water; isopropyl alcohol / 10 - 60 °C / 31789.8 Torr / Autoclave
View Scheme
Multi-step reaction with 3 steps
1.1: ozone / acetic acid methyl ester / 1.67 h / 4.9 °C
1.2: 15 - 20 °C
2.1: 5%-palladium/activated carbon; hydrogen / acetic acid methyl ester; water / 5.5 h / 15 - 25 °C / 11103.3 Torr / Autoclave
3.1: ammonium hydroxide / water; isopropyl alcohol / 10 - 60 °C / 31789.8 Torr / Autoclave
View Scheme
Multi-step reaction with 3 steps
1.1: ozone / 3.5 h / 5 °C
1.2: 5 - 20 °C
2.1: 5%-palladium/activated carbon; hydrogen / acetic acid methyl ester; water / 5.5 h / 15 - 25 °C / 11103.3 Torr / Autoclave
3.1: ammonium hydroxide / water; isopropyl alcohol / 10 - 60 °C / 31789.8 Torr / Autoclave
View Scheme
dodeca-4,8-diene-1,12-dialdehyde
55303-96-3

dodeca-4,8-diene-1,12-dialdehyde

1,12-Diaminododecane
2783-17-7

1,12-Diaminododecane

Conditions
ConditionsYield
Multi-step reaction with 2 steps
1: 5%-palladium/activated carbon; hydrogen / acetic acid methyl ester; water / 5.5 h / 15 - 25 °C / 11103.3 Torr / Autoclave
2: ammonium hydroxide / water; isopropyl alcohol / 10 - 60 °C / 31789.8 Torr / Autoclave
View Scheme
cyclododecene
1501-82-2

cyclododecene

1,12-Diaminododecane
2783-17-7

1,12-Diaminododecane

Conditions
ConditionsYield
Multi-step reaction with 2 steps
1.1: acetic acid; ozone / 2.5 h / 5 °C / Inert atmosphere
1.2: 2 h / 10 - 20 °C
2.1: ammonium hydroxide / water; isopropyl alcohol / 60 °C / 11103.3 - 31789.8 Torr / Inert atmosphere; Autoclave
View Scheme
Multi-step reaction with 2 steps
1.1: ozone / acetic acid methyl ester / 4.4 °C / Inert atmosphere
1.2: 20 °C
2.1: ammonium hydroxide / water; isopropyl alcohol / 60 °C / 11103.3 - 31789.8 Torr / Inert atmosphere; Autoclave
View Scheme
tert-butyl(12-azidododecyl)carbamate

tert-butyl(12-azidododecyl)carbamate

1,12-Diaminododecane
2783-17-7

1,12-Diaminododecane

Conditions
ConditionsYield
Multi-step reaction with 2 steps
1.1: trifluoroacetic acid / 5 h / 20 °C
2.1: trimethylphosphane / water-d2; deuteromethanol / 25 h
2.2: 24 h
View Scheme
12-azidododecan-1-amine
1416710-80-9

12-azidododecan-1-amine

1,12-Diaminododecane
2783-17-7

1,12-Diaminododecane

Conditions
ConditionsYield
Stage #1: 12-azidododecan-1-amine With trimethylphosphane In deuteromethanol; water-d2 for 25h; Staudinger Azide Reduction;
Stage #2: for 24h;
N-(tent-butoxycarbonyl)-12-bromododecylamine
887353-35-7

N-(tent-butoxycarbonyl)-12-bromododecylamine

1,12-Diaminododecane
2783-17-7

1,12-Diaminododecane

Conditions
ConditionsYield
Multi-step reaction with 3 steps
1.1: sodium azide / N,N-dimethyl-formamide / 20 h / 85 °C
2.1: trifluoroacetic acid / 5 h / 20 °C
3.1: trimethylphosphane / water-d2; deuteromethanol / 25 h
3.2: 24 h
View Scheme
1,12-dodecanedioic acid
693-23-2

1,12-dodecanedioic acid

1,12-Diaminododecane
2783-17-7

1,12-Diaminododecane

Conditions
ConditionsYield
Multi-step reaction with 2 steps
1: lithium aluminium tetrahydride / tetrahydrofuran / 0 - 20 °C
2: tris(2,4-pentanedionato)ruthenium(III); [2-((diphenylphospino)methyl)-2-methyl-1,3-propanediyl]bis[diphenylphosphine]; hydrogen; ammonia / 1,4-dioxane; water / 20 h / 220 °C / 7500.75 Torr / Autoclave; Inert atmosphere
View Scheme
Multi-step reaction with 3 steps
1: ammonium / 0.5 h / Heating
2: phosphorus pentoxide / 1 h / 15 - 37.5 Torr / Heating
3: hydrogen / ethanol / 1 h / 100 °C / 60006 Torr
View Scheme
Multi-step reaction with 3 steps
1: ammonium / 0.5 h / Heating
2: 1 h / 15 - 37.5 Torr / Heating
3: hydrogen / ethanol / 1 h / 100 °C / 60006 Torr
View Scheme
1,12-dodecandiol
5675-51-4

1,12-dodecandiol

1,12-Diaminododecane
2783-17-7

1,12-Diaminododecane

Conditions
ConditionsYield
With tris(2,4-pentanedionato)ruthenium(III); ammonia; hydrogen; [2-((diphenylphospino)methyl)-2-methyl-1,3-propanediyl]bis[diphenylphosphine] In 1,4-dioxane; water at 220℃; under 7500.75 Torr; for 20h; Temperature; Autoclave; Inert atmosphere;87 %Spectr.
1,10-decanedicarboxamide
6224-99-3

1,10-decanedicarboxamide

1,12-Diaminododecane
2783-17-7

1,12-Diaminododecane

Conditions
ConditionsYield
Multi-step reaction with 2 steps
1: phosphorus pentoxide / 1 h / 315 °C / 15001.5 - 37503.8 Torr
2: hydrogen / ethanol / 1 h / 100 °C / 60006 Torr
View Scheme
Multi-step reaction with 2 steps
1: phosphorus pentoxide / 1 h / 15 - 37.5 Torr / Heating
2: hydrogen / ethanol / 1 h / 100 °C / 60006 Torr
View Scheme
Multi-step reaction with 2 steps
1: 1 h / 15 - 37.5 Torr / Heating
2: hydrogen / ethanol / 1 h / 100 °C / 60006 Torr
View Scheme
1,12-dodecandiol
5675-51-4

1,12-dodecandiol

A

12-aminododecan-1-ol
67107-87-3

12-aminododecan-1-ol

B

1,12-Diaminododecane
2783-17-7

1,12-Diaminododecane

Conditions
ConditionsYield
With pyridoxal 5'-phosphate; MATITNHMPTAELQALDAAHHLHPFSANNALGEEGTRVITRARGVWLNDSEGEEILDAMAGLWCVNIGYGRDELAEVAARQMRELPYYNTFFKTTHVPAIALAQKLAELAPGDLNHVFFAGGGSEANDTNIRMVRTYWQNKGQPEKTVIISRKNAYHGSTVASSALGGMAGMHAQSGLIPDVHHINQPNWWAEGGDMDPEEFGLARARELEEAILELGENRVAAFIAEPVQGAGGVIVAPDSYWPEIQRICDKYDILLIADEVICGFGRTGNWFGTQTMGIRPHIMTIAKGLSSGYAPIGGSIVCDEVAHVIGKDEFNHGYTYSGHPVAAAVALENLRILEEENILDHVRNVAAPYLKEKWEALTDHPLVGEAKIVGMMASIALTPNKASRAKFASEPGTIGYICRERCFANNLIMRHVGDRMIISPPLVITPAEIDEMFVRIRKSLDEAQAEIEKQGLMKSA; MIKAYAALEANGKLQPFEYDPGALGANEVEIEVQYCGVCHSDLSMINNEWGISNYPLVPGHEVVGTVAAMGEGVNHVEVGDLVGLGWHSGYCMTCHSCLSGYHNLCATAESTIVGHYGGFGDRVRAKGVSVVKLPKGIDLASAGPLFCGGITVFSPMVELSLKPTAKVAVIGIGGLGHLAVQFLRAWGCEVTAFTSSARKQTEVLELGAHHILDSTNPEAIASAEGKFDYIISTVNLKLDWNLYISTLAPQGHFHFVGVVLEPLDLNLFPLLMGQRSVSASPVGSPATIATMLDFAVRHDIKPVVEQFSFDQINEAIAHLESGKAHYRVVLSHSKN; nicotinamide adenine dinucleotide phosphate; benzylamine In dimethyl sulfoxide at 37℃; for 24h; pH=8; Solvent; Microbiological reaction; Enzymatic reaction;
0.22C20H30N6(2-)*1.56C4H5N2(1-)*Zn(2+)

0.22C20H30N6(2-)*1.56C4H5N2(1-)*Zn(2+)

A

2-methylimidazole
693-98-1

2-methylimidazole

B

1,12-Diaminododecane
2783-17-7

1,12-Diaminododecane

C

2-imidazolecarbaldehyde
10111-08-7

2-imidazolecarbaldehyde

Conditions
ConditionsYield
With hydrogen chloride In dimethylsulfoxide-d6
1,12-Diaminododecane
2783-17-7

1,12-Diaminododecane

4-methoxy-benzoyl chloride
100-07-2

4-methoxy-benzoyl chloride

C28H40N2O4
27890-95-5

C28H40N2O4

Conditions
ConditionsYield
With triethylamine In dichloromethane at 20℃; for 2h; Inert atmosphere;100%
With potassium hydroxide In 1,2-dichloro-ethane
With potassium hydroxide
1,12-Diaminododecane
2783-17-7

1,12-Diaminododecane

1,12-dilactobionamidododecane

1,12-dilactobionamidododecane

Conditions
ConditionsYield
In methanol for 24h; Heating;100%
4,7-dichloroquinoline
86-98-6

4,7-dichloroquinoline

1,12-Diaminododecane
2783-17-7

1,12-Diaminododecane

N1-(7-Chloro-quinolin-4-yl)-dodecane-1,12-diamine
1026678-59-0

N1-(7-Chloro-quinolin-4-yl)-dodecane-1,12-diamine

Conditions
ConditionsYield
Inert atmosphere;100%
1.) 80 deg C, 1 h, 2.) 135-145 deg C, 3 h;
1,12-Diaminododecane
2783-17-7

1,12-Diaminododecane

p-phenylene-bis-4,4'-(2,6-diphenylpyrylium) p-toluenesulfonate

p-phenylene-bis-4,4'-(2,6-diphenylpyrylium) p-toluenesulfonate

polymer, product of ring-transmutation polymerization; monomer(s): 1,12-dodecane; 4,4\-(1,4-phenylene)bis(2,6-diphenylpyrilium) ditosylate

polymer, product of ring-transmutation polymerization; monomer(s): 1,12-dodecane; 4,4\-(1,4-phenylene)bis(2,6-diphenylpyrilium) ditosylate

Conditions
ConditionsYield
In dimethyl sulfoxide; toluene at 145 - 150℃; for 24h;100%
1,12-Diaminododecane
2783-17-7

1,12-Diaminododecane

2-bromophenyl isocyanate
1592-00-3

2-bromophenyl isocyanate

C26H36Br2N4O2
1373991-00-4

C26H36Br2N4O2

Conditions
ConditionsYield
In tetrahydrofuran at 20℃; for 0.25h;100%
In tetrahydrofuran at 20℃; for 0.25h;100%
1,12-Diaminododecane
2783-17-7

1,12-Diaminododecane

alpha cyclodextrin
10016-20-3

alpha cyclodextrin

2C36H60O30*C12H28N2

2C36H60O30*C12H28N2

Conditions
ConditionsYield
In water for 13h; Reflux;100%
In water at 20℃; Reflux;
In water at 20℃; Reflux;
1,12-Diaminododecane
2783-17-7

1,12-Diaminododecane

3,5-dimethylphenyl isocyanate
54132-75-1

3,5-dimethylphenyl isocyanate

C30H46N4O2
1033316-84-5

C30H46N4O2

Conditions
ConditionsYield
In tetrahydrofuran at 20℃; for 0.25h;100%
In tetrahydrofuran at 20℃; for 0.25h;100%
1,12-Diaminododecane
2783-17-7

1,12-Diaminododecane

2,3,4-tris(benzyloxy)benzoic acid
180206-32-0

2,3,4-tris(benzyloxy)benzoic acid

C68H72N2O8

C68H72N2O8

Conditions
ConditionsYield
Stage #1: 2,3,4-tris(benzyloxy)benzoic acid With benzotriazol-1-yloxyl-tris-(pyrrolidino)-phosphonium hexafluorophosphate In dichloromethane for 0.0833333h;
Stage #2: 1,12-Diaminododecane With triethylamine In dichloromethane at 20℃;
100%
1,12-Diaminododecane
2783-17-7

1,12-Diaminododecane

3,5-di-tert-butyl-2-hydroxybenzaldehyde
37942-07-7

3,5-di-tert-butyl-2-hydroxybenzaldehyde

C42H68N2O2

C42H68N2O2

Conditions
ConditionsYield
In methanol at 20℃;100%
1,12-Diaminododecane
2783-17-7

1,12-Diaminododecane

4-methyl-benzoyl chloride
874-60-2

4-methyl-benzoyl chloride

C28H40N2O2

C28H40N2O2

Conditions
ConditionsYield
With triethylamine In dichloromethane at 20℃; for 2h; Inert atmosphere;100%
1,12-Diaminododecane
2783-17-7

1,12-Diaminododecane

1,12-Dodecanediamine, dihydrochloride
3943-56-4, 15536-18-2

1,12-Dodecanediamine, dihydrochloride

Conditions
ConditionsYield
With hydrogenchloride In 1,4-dioxane; methanol for 0.166667h;100%
1,12-Diaminododecane
2783-17-7

1,12-Diaminododecane

C12H28N2*2HNO3

C12H28N2*2HNO3

Conditions
ConditionsYield
With trihydroxy amine In water100%
1,12-Diaminododecane
2783-17-7

1,12-Diaminododecane

di-tert-butyl dicarbonate
24424-99-5

di-tert-butyl dicarbonate

tert-butyl (12-aminododecyl)carbamate
109792-60-1

tert-butyl (12-aminododecyl)carbamate

Conditions
ConditionsYield
With sodium hydroxide In dichloromethane; water for 1.08333h;99%
In chloroform at 0 - 20℃;90%
In chloroform81%
morpholine
110-91-8

morpholine

1,12-Diaminododecane
2783-17-7

1,12-Diaminododecane

pentaerythritol tetraacrylate
4986-89-4

pentaerythritol tetraacrylate

C62H104N6O20

C62H104N6O20

Conditions
ConditionsYield
Stage #1: 1,12-Diaminododecane; pentaerythritol tetraacrylate In methanol at 25℃; for 18h; Michael addition;
Stage #2: morpholine In methanol at 20℃; for 18h; Further stages.;
99%
1,12-Diaminododecane
2783-17-7

1,12-Diaminododecane

geldanmycin
30562-34-6

geldanmycin

GMD-C12-dimer
301643-24-3

GMD-C12-dimer

Conditions
ConditionsYield
In N,N-dimethyl-formamide at 20℃; for 14h;98%
1,12-Diaminododecane
2783-17-7

1,12-Diaminododecane

carbonic acid dimethyl ester
616-38-6

carbonic acid dimethyl ester

N,N'-dodecanediyl-bis-carbamic acid dimethyl ester

N,N'-dodecanediyl-bis-carbamic acid dimethyl ester

Conditions
ConditionsYield
lipase from Candida antarctica In toluene at 70℃; for 19h; Product distribution / selectivity;98%
L-rhamnose
73-34-7

L-rhamnose

1,12-Diaminododecane
2783-17-7

1,12-Diaminododecane

C24H48N2O8

C24H48N2O8

Conditions
ConditionsYield
for 3h; Milling; Green chemistry;98%
1,12-Diaminododecane
2783-17-7

1,12-Diaminododecane

bis(calix[4]imidazolylidene[2]pyrazolato)octakissilver(I) tetrakis(trifluoromethanesulfonate)

bis(calix[4]imidazolylidene[2]pyrazolato)octakissilver(I) tetrakis(trifluoromethanesulfonate)

3,5-di-tert-butylbenzoic anhydride

3,5-di-tert-butylbenzoic anhydride

C42H68N2O2*C48H44Ag8N24(4+)*4CF3O3S(1-)

C42H68N2O2*C48H44Ag8N24(4+)*4CF3O3S(1-)

Conditions
ConditionsYield
Stage #1: 1,12-Diaminododecane; bis(calix[4]imidazolylidene[2]pyrazolato)octakissilver(I) tetrakis(trifluoromethanesulfonate) In N,N-dimethyl-formamide at 20℃; for 0.166667h; Schlenk technique; Inert atmosphere;
Stage #2: 3,5-di-tert-butylbenzoic anhydride With N-ethyl-N,N-diisopropylamine In N,N-dimethyl-formamide at -50 - 20℃; for 16h; Schlenk technique; Inert atmosphere;
98%
1,12-Diaminododecane
2783-17-7

1,12-Diaminododecane

acetic anhydride
108-24-7

acetic anhydride

N,N'-Diacetyl-1,12-dodecandiamin
31991-77-2

N,N'-Diacetyl-1,12-dodecandiamin

Conditions
ConditionsYield
With pyridine at 20℃;97%
1,12-Diaminododecane
2783-17-7

1,12-Diaminododecane

N-Cbz-L-Phe
1161-13-3

N-Cbz-L-Phe

1,12-dodecano-bis(L-PheZ)
182684-40-8

1,12-dodecano-bis(L-PheZ)

Conditions
ConditionsYield
Stage #1: N-Cbz-L-Phe With 1,1'-carbonyldiimidazole In chloroform at 20℃; for 1.5h;
Stage #2: 1,12-Diaminododecane In chloroform at 20℃;
97%
With dmap; dicyclohexyl-carbodiimide In chloroform for 20h; Ambient temperature;74%
1,12-Diaminododecane
2783-17-7

1,12-Diaminododecane

methyl 2-cyanoacetate
105-34-0

methyl 2-cyanoacetate

N,N'-dodecamethylenebis(2-cyanoacetamide)

N,N'-dodecamethylenebis(2-cyanoacetamide)

Conditions
ConditionsYield
In neat (no solvent) at 20℃; for 24h;97%
1,12-Diaminododecane
2783-17-7

1,12-Diaminododecane

m-anisoyl chloride
1711-05-3

m-anisoyl chloride

C28H40N2O4

C28H40N2O4

Conditions
ConditionsYield
With triethylamine In dichloromethane at 20℃; for 2h; Inert atmosphere;97%
1,12-Diaminododecane
2783-17-7

1,12-Diaminododecane

ethyl 2-(1-ethoxyethylidene)hydrazinecarboxylate
51814-82-5, 51814-83-6, 58910-28-4

ethyl 2-(1-ethoxyethylidene)hydrazinecarboxylate

C18H32N6O2

C18H32N6O2

Conditions
ConditionsYield
In water for 5.5h; Heating;96%
1,12-Diaminododecane
2783-17-7

1,12-Diaminododecane

Ethylbutyratcarbethoxyhydrazon
58910-19-3

Ethylbutyratcarbethoxyhydrazon

C22H40N6O2

C22H40N6O2

Conditions
ConditionsYield
In water for 5.5h; Heating;96%
1,12-Diaminododecane
2783-17-7

1,12-Diaminododecane

C31H60ClN5

C31H60ClN5

C43H87N7

C43H87N7

Conditions
ConditionsYield
In tetrahydrofuran Heating;96%
L-rhamnose
73-34-7

L-rhamnose

1,12-Diaminododecane
2783-17-7

1,12-Diaminododecane

C18H38N2O4

C18H38N2O4

Conditions
ConditionsYield
In neat (no solvent) for 1.5h; Milling; Green chemistry;96%
1,12-Diaminododecane
2783-17-7

1,12-Diaminododecane

Boc-Trp-OH
13139-14-5

Boc-Trp-OH

di-tert-butyl ((2S,2'S)-(dodecane-1,12-diylbis(azanediyl))bis(3-(1H-indol-3-yl)-1-oxopropane-2,1-diyl))dicarbamate

di-tert-butyl ((2S,2'S)-(dodecane-1,12-diylbis(azanediyl))bis(3-(1H-indol-3-yl)-1-oxopropane-2,1-diyl))dicarbamate

Conditions
ConditionsYield
With O-(1H-benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium hexafluorophosphate; N-ethyl-N,N-diisopropylamine In N,N-dimethyl-formamide at 20℃; Inert atmosphere;96%
Z-Leu-OH
2018-66-8

Z-Leu-OH

1,12-Diaminododecane
2783-17-7

1,12-Diaminododecane

1,12-dodecano-bis(L-LeuZ)
293732-21-5

1,12-dodecano-bis(L-LeuZ)

Conditions
ConditionsYield
Stage #1: Z-Leu-OH With 1,1'-carbonyldiimidazole In chloroform at 20℃; for 1.5h;
Stage #2: 1,12-Diaminododecane In chloroform at 20℃;
95.7%
1,12-Diaminododecane
2783-17-7

1,12-Diaminododecane

9,10-dioxo-9,10-dihydro-2-anthracenesulfonyl chloride
2381-23-9

9,10-dioxo-9,10-dihydro-2-anthracenesulfonyl chloride

C40H40N2O8S2
912278-57-0

C40H40N2O8S2

Conditions
ConditionsYield
With potassium carbonate In tetrahydrofuran; water at 60 - 65℃; for 2h;95%
1,12-Diaminododecane
2783-17-7

1,12-Diaminododecane

hexan-1-ol
111-27-3

hexan-1-ol

Hexanoic acid (12-hexanoylamino-dodecyl)-amide
58982-05-1

Hexanoic acid (12-hexanoylamino-dodecyl)-amide

Conditions
ConditionsYield
With C29H44Cl2N2Ru; potassium tert-butylate In toluene for 24h; Reflux;95%

2783-17-7Relevant articles and documents

Multi-enzymatic cascade reactions with Escherichia coli-based modules for synthesizing various bioplastic monomers from fatty acid methyl esters?

Jung, Hyunsang,Kim, Byung-Gee,Kim, Ye Chan,Park, Beom Gi,Patil, Mahesh D.,Sarak, Sharad,Yoo, Hee-Wang,Yun, Hyungdon

, p. 2222 - 2231 (2022/04/03)

Multi-enzymatic cascade reaction systems were designed to generate biopolymer monomers using Escherichia coli-based cell modules, capable of carrying out one-pot reactions. Three cell-based modules, including a ω-hydroxylation module (Cell-Hm) to convert fatty acid methyl esters (FAMEs) to ω-hydroxy fatty acids (ω-HFAs), an amination module (Cell-Am) to convert terminal alcohol groups of the substrate to amine groups, and a reduction module (Cell-Rm) to convert the carboxyl groups of fatty acids to alcohol groups, were constructed. The product-oriented assembly of these cell modules involving multi-enzymatic cascade reactions generated ω-ADAs (up to 46 mM), α,ω-diols (up to 29 mM), ω-amino alcohols (up to 29 mM) and α,ω-diamines (up to 21 mM) from 100 mM corresponding FAME substrates with varying carbon chain length (C8, C10, and C12). Finally 12-ADA and 1,12-diol were purified with isolated yields of 66.5% and 52.5%, respectively. The multi-enzymatic cascade reactions reported herein present an elegant ‘greener’ alternative for the biosynthesis of various biopolymer monomers from renewable saturated fatty acids.

Imprinted Apportionment of Functional Groups in Multivariate Metal-Organic Frameworks

Feng, Liang,Wang, Kun-Yu,Lv, Xiu-Liang,Powell, Joshua A.,Yan, Tian-Hao,Willman, Jeremy,Zhou, Hong-Cai

supporting information, p. 14524 - 14529 (2019/10/02)

Sophisticated chemical processes widely observed in biological cells require precise apportionment regulation of building units, which inspires researchers to develop tailorable architectures with controllable heterogeneity for replication, recognition and information storage. However, it remains a substantial challenge to endow multivariate materials with internal sequences and controllable apportionments. Herein, we introduce a novel strategy to manipulate the apportionment of functional groups in multivariate metal-organic frameworks (MTV-MOFs) by preincorporating interlocked linkers into framework materials. As a proof of concept, the imprinted apportionment of functional groups within ZIF-8 was achieved by exchanging imine-based linker templates with original linkers initially. The removal of linker fragments by hydrolysis can be achieved via postsynthetic labilization, leading to the formation of architectures with controlled heterogeneity. The distributions of functional groups in the resulting imprinted MOFs can be tuned by judicious control of the interlocked chain length, which was further analyzed by computational methods. This work provides synthetic tools for precise control of pore environment and functionality sequences inside multicomponent materials.

Corresponding amine nitrile and method of manufacturing thereof (by machine translation)

-

Paragraph 0152, (2018/07/15)

The present invention relates to a nitrile manufacturing method, which has characteristics of significantly-reduced ammonia source consumption, low environmental pressure, low energy consumption, low production cost, high nitrile purity, high nitrile yield and the like compared with the method in the prior art, wherein nitrile having a complicated structure can be obtained through the method. The present invention further relates to a method for producing a corresponding amine from the nitrile.

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