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629-30-1

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629-30-1 Usage

Uses

1,7-Heptanediol is used in agrochemical, pharmaceutical and dyestuff field .

Check Digit Verification of cas no

The CAS Registry Mumber 629-30-1 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 6,2 and 9 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 629-30:
(5*6)+(4*2)+(3*9)+(2*3)+(1*0)=71
71 % 10 = 1
So 629-30-1 is a valid CAS Registry Number.
InChI:InChI=1/C7H16O2/c8-6-4-2-1-3-5-7-9/h8-9H,1-7H2

629-30-1 Well-known Company Product Price

  • Brand
  • (Code)Product description
  • CAS number
  • Packaging
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  • Detail
  • Alfa Aesar

  • (L06384)  1,7-Heptanediol, 98%   

  • 629-30-1

  • 5g

  • 553.0CNY

  • Detail
  • Alfa Aesar

  • (L06384)  1,7-Heptanediol, 98%   

  • 629-30-1

  • 25g

  • 1979.0CNY

  • Detail
  • Aldrich

  • (H2201)  1,7-Heptanediol  95%

  • 629-30-1

  • H2201-10G

  • 938.34CNY

  • Detail
  • Aldrich

  • (H2201)  1,7-Heptanediol  95%

  • 629-30-1

  • H2201-25G

  • 1,680.12CNY

  • Detail

629-30-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,7-Heptanediol

1.2 Other means of identification

Product number -
Other names 1,7-DIHYDROXYHEPTANE

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:629-30-1 SDS

629-30-1Synthetic route

[4-((7-hydroxy-heptoxy)-diphenyl-methyl)phenoxy]-poly(styrene-co-divinylbenzene), copolymer 99:1, trityl loading: 1.47 mmol/g

[4-((7-hydroxy-heptoxy)-diphenyl-methyl)phenoxy]-poly(styrene-co-divinylbenzene), copolymer 99:1, trityl loading: 1.47 mmol/g

1,7-heptandiol
629-30-1

1,7-heptandiol

Conditions
ConditionsYield
With trifluoroacetic acid In dichloromethane at 20℃; for 0.5h;100%
Dimethylphenylsilane
766-77-8

Dimethylphenylsilane

7-(2-tetrahydro-2H-pyranyloxy)heptan-1-ol
81036-11-5

7-(2-tetrahydro-2H-pyranyloxy)heptan-1-ol

1,7-heptandiol
629-30-1

1,7-heptandiol

Conditions
ConditionsYield
With aluminum (III) chloride In dichloromethane at 0℃; chemoselective reaction;100%
7-(2-tetrahydro-2H-pyranyloxy)heptan-1-ol
81036-11-5

7-(2-tetrahydro-2H-pyranyloxy)heptan-1-ol

1,7-heptandiol
629-30-1

1,7-heptandiol

Conditions
ConditionsYield
With acide phosphorique at 180 - 200℃;98.6%
diethyl pimelate
2050-20-6

diethyl pimelate

1,7-heptandiol
629-30-1

1,7-heptandiol

Conditions
ConditionsYield
With sodium bis(2-methoxyethoxy)aluminium dihydride In 2-methyltetrahydrofuran at 45℃; for 5h; Inert atmosphere;98%
With samarium diiodide; water; triethylamine In tetrahydrofuran at 20℃; for 20h; Inert atmosphere;87%
With ethanol; sodium
dimethyl 1,7-heptanedioate
1732-08-7

dimethyl 1,7-heptanedioate

1,7-heptandiol
629-30-1

1,7-heptandiol

Conditions
ConditionsYield
With lithium aluminium tetrahydride In tetrahydrofuran at 5 - 20℃; for 2.5h; Large scale;95.3%
With ethanol; sodium
With sodium; butan-1-ol
With lithium aluminium tetrahydride; diethyl ether
acetic acid 7-(4-methoxy-benzyloxy)-heptyl ester

acetic acid 7-(4-methoxy-benzyloxy)-heptyl ester

1,7-heptandiol
629-30-1

1,7-heptandiol

Conditions
ConditionsYield
With carbon tetrabromide In methanol for 3h; Deacetylation; ether cleavage; Heating;74%
7-hydroxyheptyl phenyl telluride
1192601-85-6

7-hydroxyheptyl phenyl telluride

A

1,7-heptandiol
629-30-1

1,7-heptandiol

B

6-hepten-1-ol
4117-10-6

6-hepten-1-ol

C

7-hydroxyheptanal
22054-13-3

7-hydroxyheptanal

Conditions
ConditionsYield
With oxygen In hexane for 0.0333333h; UV-irradiation;A 16 %Chromat.
B 6 %Chromat.
C 72%
chlorotriisopropylsilane
6485-79-6

chlorotriisopropylsilane

7-(2-tetrahydro-2H-pyranyloxy)heptan-1-ol
81036-11-5

7-(2-tetrahydro-2H-pyranyloxy)heptan-1-ol

A

1,7-heptandiol
629-30-1

1,7-heptandiol

B

7-((triisopropylsilyl)oxy)heptan-1-ol
859509-85-6

7-((triisopropylsilyl)oxy)heptan-1-ol

Conditions
ConditionsYield
With aluminum (III) chloride In toluene at 0℃; chemoselective reaction;A n/a
B 58%
formaldehyd
50-00-0

formaldehyd

1,5-dibromo-pentane
111-24-0

1,5-dibromo-pentane

1,7-heptandiol
629-30-1

1,7-heptandiol

Conditions
ConditionsYield
Stage #1: 1,5-dibromo-pentane With magnesium In tetrahydrofuran at 200℃; for 2h; Inert atmosphere;
Stage #2: formaldehyd In tetrahydrofuran for 12h;
50%
heptanedioic acid
111-16-0

heptanedioic acid

1,7-heptandiol
629-30-1

1,7-heptandiol

Conditions
ConditionsYield
With potassium hydroxide; samarium diiodide In tetrahydrofuran; water for 0.01h; Ambient temperature;25%
With lithium aluminium tetrahydride; diethyl ether
With copper-aluminium-zinc catalyst at 280℃; under 147102 Torr; Hydrogenation;
Multi-step reaction with 2 steps
1: concentrated sulfuric acid
2: sodium; alcohol
View Scheme
Multi-step reaction with 2 steps
1: toluene-4-sulfonic acid / 7 h / Reflux; Large scale
2: lithium aluminium tetrahydride / tetrahydrofuran / 2.5 h / 5 - 20 °C / Large scale
View Scheme
3-furan-2-yl-propenal
623-30-3

3-furan-2-yl-propenal

1,7-heptandiol
629-30-1

1,7-heptandiol

Conditions
ConditionsYield
With hydrogen In butan-1-ol at 150℃; under 7500.75 Torr; for 4h; Autoclave;9%
3-furan-2-yl-propenal
623-30-3

3-furan-2-yl-propenal

A

1,7-heptandiol
629-30-1

1,7-heptandiol

B

1,4-heptane-diol
40646-07-9

1,4-heptane-diol

Conditions
ConditionsYield
With hydrogen In butan-1-ol at 150℃; under 7500.75 Torr; for 8h; Autoclave;A 7%
B 6%
1,7-dimethoxyheptane
137333-33-6

1,7-dimethoxyheptane

1,7-heptandiol
629-30-1

1,7-heptandiol

Conditions
ConditionsYield
With hydrogen iodide
1,7-dibromoheptane
4549-31-9

1,7-dibromoheptane

1,7-heptandiol
629-30-1

1,7-heptandiol

Conditions
ConditionsYield
With silver(I) acetate Destillierung das Diacetat ueber Natronkalk;
3-heptene-1,7-diol
84143-36-2

3-heptene-1,7-diol

1,7-heptandiol
629-30-1

1,7-heptandiol

Conditions
ConditionsYield
Hydrogenation;
hept-3-yne-1,7-diol
102547-94-4

hept-3-yne-1,7-diol

1,7-heptandiol
629-30-1

1,7-heptandiol

Conditions
ConditionsYield
With methanol; nickel under 22065.2 - 36775.4 Torr; Hydrogenation;
trimethylene oxide
503-30-0

trimethylene oxide

4-<(tetrahydropyran-2-yl)oxy>butylmagnesium chloride
58766-02-2

4-<(tetrahydropyran-2-yl)oxy>butylmagnesium chloride

1,7-heptandiol
629-30-1

1,7-heptandiol

2,8-dihydroxy-octanoic acid
66997-43-1

2,8-dihydroxy-octanoic acid

1,7-heptandiol
629-30-1

1,7-heptandiol

Conditions
ConditionsYield
With chromium(VI) oxide
oxocan-2-one
539-87-7

oxocan-2-one

1,7-heptandiol
629-30-1

1,7-heptandiol

Conditions
ConditionsYield
With lithium triethylborohydride In various solvent(s) for 0.416667h; Thermodynamic data; ΔH;
1,6-heptadiene
3070-53-9

1,6-heptadiene

A

1,7-heptandiol
629-30-1

1,7-heptandiol

B

heptane-1,5-diol
60096-09-5

heptane-1,5-diol

C

cis-1,5-cyclooctanediol
23418-82-8

cis-1,5-cyclooctanediol

Conditions
ConditionsYield
With 9-borabicyclo[3.3.1]nonane dimer; dimethylsulfide borane complex Product distribution;
3--acrolein

3--acrolein

1,7-heptandiol
629-30-1

1,7-heptandiol

Conditions
ConditionsYield
With copper chromite; ethanol at 200℃; under 73550.8 - 147102 Torr; Hydrogenation;
pimelic acid dibutyl ester

pimelic acid dibutyl ester

1,7-heptandiol
629-30-1

1,7-heptandiol

Conditions
ConditionsYield
With copper oxide-chromium oxide at 210℃; under 760000 Torr; Hydrogenation;
diethyl pimelate
2050-20-6

diethyl pimelate

ethanol
64-17-5

ethanol

sodium

sodium

1,7-heptandiol
629-30-1

1,7-heptandiol

(chloro-6' hexyloxy)-2 tetrahydropyranne
2009-84-9

(chloro-6' hexyloxy)-2 tetrahydropyranne

1,7-heptandiol
629-30-1

1,7-heptandiol

Conditions
ConditionsYield
Multi-step reaction with 2 steps
1: 1.) magnesium / 1.) THF, reflux, 1.5 h, 2.) reflux, 1 h.
2: 98.6 percent / acide phosphorique / 180 - 200 °C
View Scheme
6-chloro-1-hexanol
2009-83-8

6-chloro-1-hexanol

1,7-heptandiol
629-30-1

1,7-heptandiol

Conditions
ConditionsYield
Multi-step reaction with 3 steps
2: 1.) magnesium / 1.) THF, reflux, 1.5 h, 2.) reflux, 1 h.
3: 98.6 percent / acide phosphorique / 180 - 200 °C
View Scheme
Multi-step reaction with 2 steps
1: (i) /BRN= 4652394/, DMSO, (ii) H2, Raney-Ni, semicarbazide*HCl, aq. EtOH, (iii) /BRN= 4652394/, aq. HCl, dioxane, (iv) (heating)
2: CrO3
View Scheme
7-(tetrahydro-2H-pyran-2-yloxy)hept-3-yn-1-ol
21890-96-0

7-(tetrahydro-2H-pyran-2-yloxy)hept-3-yn-1-ol

1,7-heptandiol
629-30-1

1,7-heptandiol

Conditions
ConditionsYield
Multi-step reaction with 2 steps
1: methanol; toluene-4-sulfonic acid
2: Raney nickel; methanol / 22065.2 - 36775.4 Torr / Hydrogenation
View Scheme
pent-1-yn-5-ol
5390-04-5

pent-1-yn-5-ol

1,7-heptandiol
629-30-1

1,7-heptandiol

Conditions
ConditionsYield
Multi-step reaction with 3 steps
1: phosphoryl chloride; sodium amide; liquid ammonia / Reagens Nr. 4: Aether
2: methanol; toluene-4-sulfonic acid
3: Raney nickel; methanol / 22065.2 - 36775.4 Torr / Hydrogenation
View Scheme
B-methoxyborocane
60579-50-2

B-methoxyborocane

1,7-heptandiol
629-30-1

1,7-heptandiol

Conditions
ConditionsYield
With dihydrogen peroxide In water oxidation with alkaline H2O2;;
C6H11OPol

C6H11OPol

carbon monoxide
201230-82-2

carbon monoxide

A

1,7-heptandiol
629-30-1

1,7-heptandiol

B

(+/-)-2-methylhexane-1,6-diol
25258-92-8

(+/-)-2-methylhexane-1,6-diol

Conditions
ConditionsYield
Stage #1: C6H11OPol; carbon monoxide With acetylacetonatodicarbonylrhodium(l); hydrogen In toluene at 60℃; under 30003 Torr; for 24h; Inert atmosphere; Autoclave; solid phase reaction;
Stage #2: With sodium tetrahydroborate Inert atmosphere; solid phase reaction;
Stage #3: With trifluoroacetic acid In dichloromethane at 20℃; for 0.166667h; Inert atmosphere; solid phase reaction;
1,7-heptandiol
629-30-1

1,7-heptandiol

1,7-dichloroheptane
821-76-1

1,7-dichloroheptane

Conditions
ConditionsYield
With Ethyl trichloroacetate; triphenylphosphine In acetonitrile at 10 - 15℃; for 3h;100%
With pyridine; thionyl chloride
(i) COCl2, (ii) Ph3P; Multistep reaction;
With pyridine; thionyl chloride
1,7-heptandiol
629-30-1

1,7-heptandiol

A

pimelaldehyde
53185-69-6

pimelaldehyde

B

undeca-1,10-diene-3,9-diol
103984-88-9

undeca-1,10-diene-3,9-diol

Conditions
ConditionsYield
A 100%
B n/a
1,7-heptandiol
629-30-1

1,7-heptandiol

acetylene
74-86-2

acetylene

1,7-divinyloxyheptane
143458-13-3

1,7-divinyloxyheptane

Conditions
ConditionsYield
With potassium hydroxide; dimethyl sulfoxide at 100℃; under 760 Torr; for 5h;99%
With sodium hydroxide; cesium fluoride In dimethyl sulfoxide at 100℃; for 2.5h; atmospheric pressure;87%
1,7-heptandiol
629-30-1

1,7-heptandiol

trityl chloride
76-83-5

trityl chloride

C45H44O2
1198081-86-5

C45H44O2

Conditions
ConditionsYield
With iron(III) chloride; 1-(n-butyl)-3-methylimidazolium triflate at 40℃; for 3.16667h; Ionic liquid;99%
1,7-heptandiol
629-30-1

1,7-heptandiol

3-vinylbenzoic acid
28447-20-3

3-vinylbenzoic acid

heptane-1,7-diyl bis(3-vinylbenzoate)

heptane-1,7-diyl bis(3-vinylbenzoate)

Conditions
ConditionsYield
With dmap; dicyclohexyl-carbodiimide In dichloromethane at 20℃; for 15h; Steglich Esterification; Inert atmosphere;99%
1,7-heptandiol
629-30-1

1,7-heptandiol

heptanedioic acid
111-16-0

heptanedioic acid

Conditions
ConditionsYield
With C24H33IrN4O3; water; sodium hydroxide for 18h; Reflux;97%
azelaic acid
123-99-9

azelaic acid

1,7-heptandiol
629-30-1

1,7-heptandiol

1,9-dioxacyclooctadecane-10,18-dione
660-63-9

1,9-dioxacyclooctadecane-10,18-dione

Conditions
ConditionsYield
With hafnium(IV) trifluoromethanesulfonate In toluene at 110℃; for 48h; Inert atmosphere;96%
1,7-heptandiol
629-30-1

1,7-heptandiol

1,7-dibromoheptane
4549-31-9

1,7-dibromoheptane

Conditions
ConditionsYield
With 1-(ω-sulfonic acid)propyl-3-methylimidazolium bromide at 100℃; Inert atmosphere;95%
With dibromotriphenylphosphorane89%
With phosphorus tribromide; triethylamine In diethyl ether at 0℃;48%
1,7-heptandiol
629-30-1

1,7-heptandiol

1,1'-carbonyldiimidazole
530-62-1

1,1'-carbonyldiimidazole

heptane-1,7-diyl bis(1H-imidazole-1-carboxylate)

heptane-1,7-diyl bis(1H-imidazole-1-carboxylate)

Conditions
ConditionsYield
In dichloromethane at 20℃; Inert atmosphere;95%
1,7-heptandiol
629-30-1

1,7-heptandiol

(1S,5R,7S)-1,5,7-Trimethyl-2,4-dioxo-3-aza-bicyclo[3.3.1]nonane-7-carbonyl chloride
109216-50-4

(1S,5R,7S)-1,5,7-Trimethyl-2,4-dioxo-3-aza-bicyclo[3.3.1]nonane-7-carbonyl chloride

C31H46N2O8
129786-97-6

C31H46N2O8

Conditions
ConditionsYield
With dmap; triethylamine In dichloromethane Heating;94%
[4-((7-hydroxy-heptoxy)-diphenyl-methyl)phenoxy]-poly(styrene-co-divinylbenzene), copolymer 99:1, trityl loading: 1.47 mmol/g

[4-((7-hydroxy-heptoxy)-diphenyl-methyl)phenoxy]-poly(styrene-co-divinylbenzene), copolymer 99:1, trityl loading: 1.47 mmol/g

1,7-heptandiol
629-30-1

1,7-heptandiol

Conditions
ConditionsYield
With trifluoroacetic acid In dichloromethane at 20℃; for 0.5h;100%
Dimethylphenylsilane
766-77-8

Dimethylphenylsilane

7-(2-tetrahydro-2H-pyranyloxy)heptan-1-ol
81036-11-5

7-(2-tetrahydro-2H-pyranyloxy)heptan-1-ol

1,7-heptandiol
629-30-1

1,7-heptandiol

Conditions
ConditionsYield
With aluminum (III) chloride In dichloromethane at 0℃; chemoselective reaction;100%
7-(2-tetrahydro-2H-pyranyloxy)heptan-1-ol
81036-11-5

7-(2-tetrahydro-2H-pyranyloxy)heptan-1-ol

1,7-heptandiol
629-30-1

1,7-heptandiol

Conditions
ConditionsYield
With acide phosphorique at 180 - 200℃;98.6%
diethyl pimelate
2050-20-6

diethyl pimelate

1,7-heptandiol
629-30-1

1,7-heptandiol

Conditions
ConditionsYield
With sodium bis(2-methoxyethoxy)aluminium dihydride In 2-methyltetrahydrofuran at 45℃; for 5h; Inert atmosphere;98%
With samarium diiodide; water; triethylamine In tetrahydrofuran at 20℃; for 20h; Inert atmosphere;87%
With ethanol; sodium
dimethyl 1,7-heptanedioate
1732-08-7

dimethyl 1,7-heptanedioate

1,7-heptandiol
629-30-1

1,7-heptandiol

Conditions
ConditionsYield
With lithium aluminium tetrahydride In tetrahydrofuran at 5 - 20℃; for 2.5h; Large scale;95.3%
With ethanol; sodium
With sodium; butan-1-ol
With lithium aluminium tetrahydride; diethyl ether
acetic acid 7-(4-methoxy-benzyloxy)-heptyl ester

acetic acid 7-(4-methoxy-benzyloxy)-heptyl ester

1,7-heptandiol
629-30-1

1,7-heptandiol

Conditions
ConditionsYield
With carbon tetrabromide In methanol for 3h; Deacetylation; ether cleavage; Heating;74%
7-hydroxyheptyl phenyl telluride
1192601-85-6

7-hydroxyheptyl phenyl telluride

A

1,7-heptandiol
629-30-1

1,7-heptandiol

B

6-hepten-1-ol
4117-10-6

6-hepten-1-ol

C

7-hydroxyheptanal
22054-13-3

7-hydroxyheptanal

Conditions
ConditionsYield
With oxygen In hexane for 0.0333333h; UV-irradiation;A 16 %Chromat.
B 6 %Chromat.
C 72%
chlorotriisopropylsilane
6485-79-6

chlorotriisopropylsilane

7-(2-tetrahydro-2H-pyranyloxy)heptan-1-ol
81036-11-5

7-(2-tetrahydro-2H-pyranyloxy)heptan-1-ol

A

1,7-heptandiol
629-30-1

1,7-heptandiol

B

7-((triisopropylsilyl)oxy)heptan-1-ol
859509-85-6

7-((triisopropylsilyl)oxy)heptan-1-ol

Conditions
ConditionsYield
With aluminum (III) chloride In toluene at 0℃; chemoselective reaction;A n/a
B 58%
formaldehyd
50-00-0

formaldehyd

1,5-dibromo-pentane
111-24-0

1,5-dibromo-pentane

1,7-heptandiol
629-30-1

1,7-heptandiol

Conditions
ConditionsYield
Stage #1: 1,5-dibromo-pentane With magnesium In tetrahydrofuran at 200℃; for 2h; Inert atmosphere;
Stage #2: formaldehyd In tetrahydrofuran for 12h;
50%
heptanedioic acid
111-16-0

heptanedioic acid

1,7-heptandiol
629-30-1

1,7-heptandiol

Conditions
ConditionsYield
With potassium hydroxide; samarium diiodide In tetrahydrofuran; water for 0.01h; Ambient temperature;25%
With lithium aluminium tetrahydride; diethyl ether
With copper-aluminium-zinc catalyst at 280℃; under 147102 Torr; Hydrogenation;
Multi-step reaction with 2 steps
1: concentrated sulfuric acid
2: sodium; alcohol
View Scheme
Multi-step reaction with 2 steps
1: toluene-4-sulfonic acid / 7 h / Reflux; Large scale
2: lithium aluminium tetrahydride / tetrahydrofuran / 2.5 h / 5 - 20 °C / Large scale
View Scheme
3-furan-2-yl-propenal
623-30-3

3-furan-2-yl-propenal

1,7-heptandiol
629-30-1

1,7-heptandiol

Conditions
ConditionsYield
With hydrogen In butan-1-ol at 150℃; under 7500.75 Torr; for 4h; Autoclave;9%
3-furan-2-yl-propenal
623-30-3

3-furan-2-yl-propenal

A

1,7-heptandiol
629-30-1

1,7-heptandiol

B

1,4-heptane-diol
40646-07-9

1,4-heptane-diol

Conditions
ConditionsYield
With hydrogen In butan-1-ol at 150℃; under 7500.75 Torr; for 8h; Autoclave;A 7%
B 6%
1,7-dimethoxyheptane
137333-33-6

1,7-dimethoxyheptane

1,7-heptandiol
629-30-1

1,7-heptandiol

Conditions
ConditionsYield
With hydrogen iodide
1,7-dibromoheptane
4549-31-9

1,7-dibromoheptane

1,7-heptandiol
629-30-1

1,7-heptandiol

Conditions
ConditionsYield
With silver(I) acetate Destillierung das Diacetat ueber Natronkalk;
3-heptene-1,7-diol
84143-36-2

3-heptene-1,7-diol

1,7-heptandiol
629-30-1

1,7-heptandiol

Conditions
ConditionsYield
Hydrogenation;
hept-3-yne-1,7-diol
102547-94-4

hept-3-yne-1,7-diol

1,7-heptandiol
629-30-1

1,7-heptandiol

Conditions
ConditionsYield
With methanol; nickel under 22065.2 - 36775.4 Torr; Hydrogenation;
trimethylene oxide
503-30-0

trimethylene oxide

4-<(tetrahydropyran-2-yl)oxy>butylmagnesium chloride
58766-02-2

4-<(tetrahydropyran-2-yl)oxy>butylmagnesium chloride

1,7-heptandiol
629-30-1

1,7-heptandiol

2,8-dihydroxy-octanoic acid
66997-43-1

2,8-dihydroxy-octanoic acid

1,7-heptandiol
629-30-1

1,7-heptandiol

Conditions
ConditionsYield
With chromium(VI) oxide
oxocan-2-one
539-87-7

oxocan-2-one

1,7-heptandiol
629-30-1

1,7-heptandiol

Conditions
ConditionsYield
With lithium triethylborohydride In various solvent(s) for 0.416667h; Thermodynamic data; ΔH;
1,6-heptadiene
3070-53-9

1,6-heptadiene

A

1,7-heptandiol
629-30-1

1,7-heptandiol

B

heptane-1,5-diol
60096-09-5

heptane-1,5-diol

C

cis-1,5-cyclooctanediol
23418-82-8

cis-1,5-cyclooctanediol

Conditions
ConditionsYield
With 9-borabicyclo[3.3.1]nonane dimer; dimethylsulfide borane complex Product distribution;
3--acrolein

3--acrolein

1,7-heptandiol
629-30-1

1,7-heptandiol

Conditions
ConditionsYield
With copper chromite; ethanol at 200℃; under 73550.8 - 147102 Torr; Hydrogenation;

629-30-1Relevant articles and documents

Hydroformylation reaction ligand, hydroformylation catalyst and diol preparation method

-

Paragraph 0079-0080, (2021/06/22)

The invention discloses a hydroformylation reaction ligand, a hydroformylation catalyst and a diol preparation method According to the invention, the structural formula of the hydroformylation reaction ligand is shown in the specification, wherein R1 and R2 are mutually independent one of H, aryl or substituted aryl, thienyl, pyrrolyl, thiazolyl, imidazolyl and pyridyl; the ligand disclosed by the invention is high in catalytic activity and good in metal active center stability, by-products of aldehyde in a conventional hydroformylation reaction can be reduced, and linear diol with a high normal/isomer ratio can be obtained by a one-step method; and the method has the advantages of simple and convenient process, low cost and energy consumption, good production safety, high product quality and the like, and is particularly suitable for large-scale industrial production.

One-pot biosynthesis of 1,6-hexanediol from cyclohexane by: De novo designed cascade biocatalysis

Kang, Lixin,Li, Aitao,Li, Qian,Li, Renjie,Wang, Fei,Yu, Xiaojuan,Zhang, Zhongwei,Zhao, Jing

, p. 7476 - 7483 (2020/11/23)

1,6-Hexanediol (HDO) is an important precursor in the polymer industry. The current industrial route to produce HDO involves energy intensive and hazardous multistage (four-pot-four-step) chemical reactions using cyclohexane (CH) as the starting material, which leads to serious environmental problems. Here, we report the development of a biocatalytic cascade process for the biotransformation of CH to HDO under mild conditions in a one-pot-one-step manner. This cascade biocatalysis operates by using a microbial consortium composed of three E. coli cell modules, each containing the necessary enzymes. The cell modules with assigned functions were engineered in parallel, followed by combination to construct E. coli consortia for use in biotransformations. The engineered E. coli consortia, which contained the corresponding cell modules, efficiently converted not only CH or cyclohexanol to HDO, but also other cycloalkanes or cycloalkanols to related dihydric alcohols. In conclusion, the newly developed biocatalytic process provides a promising alternative to the current industrial process for manufacturing HDO and related dihydric alcohols. This journal is

A smarter approach to catalysts by design: Combining surface organometallic chemistry on oxide and metal gives selective catalysts for dehydrogenation of 2,3-dimethylbutane

Rouge, Pascal,Garron, Anthony,Norsic, Sébastien,Larabi, Cherif,Merle, Nicolas,Delevoye, Laurent,Gauvin, Regis M.,Szeto, Kai C.,Taoufik, Mostafa

, p. 21 - 26 (2019/04/25)

2,3-dimethylbutane is selectively converted into 2,3-dimethylbutenes at 500 °C under hydrogen or at 390 °C under nitrogen in the presence of bimetallic catalysts Pt-Sn/Li-Al2O3. The high stability of the catalyst along the reaction is obtained by selective modification of the Pt/Li-Al2O3 catalyst using Surface Organometallic Chemistry (SOMC).

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