Welcome to LookChem.com Sign In|Join Free

CAS

  • or

10340-22-4

Post Buying Request

10340-22-4 Suppliers

Recommended suppliersmore

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

10340-22-4 Usage

Uses

(3Z)-Decen-1-ol can be used as reactant/reagent in studies of influence of the Chemical Structure on Odor Qualities and Odor Thresholds in Homologous Series of Alka-1,5-dien-3-ones, Alk-1-en-3-ones, Alka-1,5-dien-3-ols, and Alk-1-en-3-ols.

Check Digit Verification of cas no

The CAS Registry Mumber 10340-22-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,0,3,4 and 0 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 10340-22:
(7*1)+(6*0)+(5*3)+(4*4)+(3*0)+(2*2)+(1*2)=44
44 % 10 = 4
So 10340-22-4 is a valid CAS Registry Number.
InChI:InChI=1/C10H20O/c1-2-3-4-5-6-7-8-9-10-11/h7-8,11H,2-6,9-10H2,1H3/b8-7-

10340-22-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name (3Z)-3-Decen-1-ol

1.2 Other means of identification

Product number -
Other names 2-Propenoic acid,3-cyclohexyl-,(2Z)

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:10340-22-4 SDS

10340-22-4Synthetic route

3-decyn-1-ol
51721-39-2

3-decyn-1-ol

(Z)-dec-3-en-1-ol
10340-22-4

(Z)-dec-3-en-1-ol

Conditions
ConditionsYield
With hydrogen In N,N-dimethyl-formamide at 40℃; for 4h; Schlenk technique;93%
With sodium tetrahydroborate; hydrogen; nickel(II) acetate tetrahydrate In ethanol at 20℃; for 12h;91%
With quinoline; hydrogen; Lindlar's catalyst In hexane under 760 Torr; Ambient temperature;86%
(Z)-1-(2-tetrahydropyranyloxy)-dec-3-ene
137103-87-8

(Z)-1-(2-tetrahydropyranyloxy)-dec-3-ene

(Z)-dec-3-en-1-ol
10340-22-4

(Z)-dec-3-en-1-ol

Conditions
ConditionsYield
With toluene-4-sulfonic acid In methanol for 6h; Ambient temperature;82%
2,3-dihydro-2H-furan
1191-99-7

2,3-dihydro-2H-furan

n-hexylmagnesium bromide
3761-92-0

n-hexylmagnesium bromide

(Z)-dec-3-en-1-ol
10340-22-4

(Z)-dec-3-en-1-ol

Conditions
ConditionsYield
Stage #1: 2,3-dihydro-2H-furan With bis(1,5-cyclooctadiene)nickel(0); C27H39N2(1+)*Cl(1-)*ClH; lithium chloride In tetrahydrofuran at -30℃; for 0.0333333h; Inert atmosphere;
Stage #2: n-hexylmagnesium bromide In tetrahydrofuran at -30℃; for 16h; Inert atmosphere; stereoselective reaction;
47%
heptanal
111-71-7

heptanal

3-hydroxypropyltriphenylphosphonium bromide
51860-45-8

3-hydroxypropyltriphenylphosphonium bromide

A

(Z)-dec-3-en-1-ol
10340-22-4

(Z)-dec-3-en-1-ol

B

trans-3-decen-1-ol
10339-60-3

trans-3-decen-1-ol

Conditions
ConditionsYield
With phenyllithium 1.) THF/diethyl ether, 20 min, 2.) -75 deg C, 15 min, -30 deg C, 30 min, 25 deg C; Yield given. Multistep reaction. Yields of byproduct given. Title compound not separated from byproducts;
1,4-decadien-3-ol
138041-89-1

1,4-decadien-3-ol

A

(Z)-dec-3-en-1-ol
10340-22-4

(Z)-dec-3-en-1-ol

B

(Z)-2-decen-5-ol
137256-01-0

(Z)-2-decen-5-ol

Conditions
ConditionsYield
With ammonium molybdate; hydrogen; chromium(0) hexacarbonyl 1.) o-xylene, reflux, 30 min., 2.) hexane, 160-180 deg C, 50-80 atm; Yield given. Multistep reaction. Yields of byproduct given;
n-octyne
629-05-0

n-octyne

(Z)-dec-3-en-1-ol
10340-22-4

(Z)-dec-3-en-1-ol

Conditions
ConditionsYield
Multi-step reaction with 2 steps
1: 1.96 g / n-butyl lithium, boron trifluoride etherate / hexane; tetrahydrofuran / 0.5 h / -78 °C
2: 0.75 g / hydrogen, quinoline / Pd-CaCO3 / hexane
View Scheme
Multi-step reaction with 2 steps
1.1: ethylmagnesium bromide / tetrahydrofuran / Reflux
1.2: 20 °C
2.1: nickel(II) acetate tetrahydrate; sodium tetrahydroborate; hydrogen / ethanol / 12 h / 20 °C
View Scheme
(Z)-dec-3-en-1-ol
10340-22-4

(Z)-dec-3-en-1-ol

(Z)-dec-3-enoic acid
2430-93-5

(Z)-dec-3-enoic acid

Conditions
ConditionsYield
With dipyridinium dichromate In N,N-dimethyl-formamide for 14h; Ambient temperature;67%
With potassium dichromate; sodium periodate; nitric acid In water; acetonitrile at 0 - 20℃; for 12h;37%
With chromium(VI) oxide; periodic acid In water; acetonitrile at 0 - 5℃;
(Z)-dec-3-en-1-ol
10340-22-4

(Z)-dec-3-en-1-ol

methanesulfonyl chloride
124-63-0

methanesulfonyl chloride

Methanesulfonic acid (Z)-dec-3-enyl ester

Methanesulfonic acid (Z)-dec-3-enyl ester

Conditions
ConditionsYield
With triethylamine In dichloromethane
With triethylamine In dichloromethane at 0℃;
6-dodecyne
6975-99-1

6-dodecyne

(Z)-dec-3-en-1-ol
10340-22-4

(Z)-dec-3-en-1-ol

A

(E)-4-Hexyl-5-pentyl-undec-5-en-1-ol

(E)-4-Hexyl-5-pentyl-undec-5-en-1-ol

B

(E)-3-Heptyl-4-pentyl-dec-4-en-1-ol

(E)-3-Heptyl-4-pentyl-dec-4-en-1-ol

Conditions
ConditionsYield
Yield given. Multistep reaction. Yields of byproduct given. Title compound not separated from byproducts;
(Z)-dec-3-en-1-ol
10340-22-4

(Z)-dec-3-en-1-ol

(Z)-1-bromdec-3-ene
72855-89-1

(Z)-1-bromdec-3-ene

Conditions
ConditionsYield
With carbon tetrabromide; triphenylphosphine In tetrahydrofuran Substitution;
Multi-step reaction with 2 steps
1: triethylamine / dichloromethane / 0 °C
2: lithium bromide / acetone / 3 h / Reflux
View Scheme
(Z)-dec-3-en-1-ol
10340-22-4

(Z)-dec-3-en-1-ol

(Z)-3-decenal
69891-94-7

(Z)-3-decenal

Conditions
ConditionsYield
With [bis(acetoxy)iodo]benzene; TEMPO on colloidal silica In dichloromethane; pentane at 20℃;
With Dess-Martin periodane In dichloromethane at 20℃; for 3h; Dess-Martin Oxidation;
With Dess-Martin periodane In dichloromethane at 20℃; for 3h;
With Dess-Martin periodane In dichloromethane at 20℃; for 3.08h;
(Z)-dec-3-en-1-ol
10340-22-4

(Z)-dec-3-en-1-ol

(Z)-dodec-5-en-1-yne

(Z)-dodec-5-en-1-yne

Conditions
ConditionsYield
Multi-step reaction with 2 steps
1: CBr4; Ph3P / tetrahydrofuran
2: tetrahydrofuran; hexamethylphosphoric acid triamide
View Scheme
Multi-step reaction with 3 steps
1: triethylamine / dichloromethane / 0 °C
2: lithium bromide / acetone / 3 h / Reflux
3: dimethyl sulfoxide / 12 h / 0 - 23 °C
View Scheme
(Z)-dec-3-en-1-ol
10340-22-4

(Z)-dec-3-en-1-ol

(3E,7Z)-3,7-tetradecadienol

(3E,7Z)-3,7-tetradecadienol

Conditions
ConditionsYield
Multi-step reaction with 4 steps
1: CBr4; Ph3P / tetrahydrofuran
2: tetrahydrofuran; hexamethylphosphoric acid triamide
3: n-BuLi / hexamethylphosphoric acid triamide
4: LiAlH4 / tetrahydrofuran; bis-(2-methoxy-ethyl) ether
View Scheme
(Z)-dec-3-en-1-ol
10340-22-4

(Z)-dec-3-en-1-ol

(Z)-Tetradec-7-en-3-yn-1-ol

(Z)-Tetradec-7-en-3-yn-1-ol

Conditions
ConditionsYield
Multi-step reaction with 3 steps
1: CBr4; Ph3P / tetrahydrofuran
2: tetrahydrofuran; hexamethylphosphoric acid triamide
3: n-BuLi / hexamethylphosphoric acid triamide
View Scheme
(Z)-dec-3-en-1-ol
10340-22-4

(Z)-dec-3-en-1-ol

(E,Z)-3,7-Tetradecadien-1-ol acetate

(E,Z)-3,7-Tetradecadien-1-ol acetate

Conditions
ConditionsYield
Multi-step reaction with 5 steps
1: CBr4; Ph3P / tetrahydrofuran
2: tetrahydrofuran; hexamethylphosphoric acid triamide
3: n-BuLi / hexamethylphosphoric acid triamide
4: LiAlH4 / tetrahydrofuran; bis-(2-methoxy-ethyl) ether
5: acetic acid
View Scheme
(Z)-dec-3-en-1-ol
10340-22-4

(Z)-dec-3-en-1-ol

(Z)-12-nonadecen-9-one
63408-45-7

(Z)-12-nonadecen-9-one

Conditions
ConditionsYield
Multi-step reaction with 4 steps
1: triethylamine / CH2Cl2
2: 0.9 g / NaI / acetone / 3 h
3: 0.31 g / NaH / dimethylsulfoxide; diethyl ether / 3 h / Ambient temperature
4: 0.18 g / conc. hydrochloric acid / CH2Cl2; diethyl ether / 0.25 h / 25 °C
View Scheme
(Z)-dec-3-en-1-ol
10340-22-4

(Z)-dec-3-en-1-ol

(13Z)-eicos-13-en-10-one
63408-44-6

(13Z)-eicos-13-en-10-one

Conditions
ConditionsYield
Multi-step reaction with 4 steps
1: triethylamine / CH2Cl2
2: 0.9 g / NaI / acetone / 3 h
3: 0.180 g / NaH / dimethylsulfoxide; diethyl ether
4: conc. hydrochloric acid / CH2Cl2; diethyl ether
View Scheme
(Z)-dec-3-en-1-ol
10340-22-4

(Z)-dec-3-en-1-ol

(Z)-3-decenyl iodide
88338-57-2

(Z)-3-decenyl iodide

Conditions
ConditionsYield
Multi-step reaction with 2 steps
1: triethylamine / CH2Cl2
2: 0.9 g / NaI / acetone / 3 h
View Scheme
(Z)-dec-3-en-1-ol
10340-22-4

(Z)-dec-3-en-1-ol

1-((Z)-9-Isocyano-nonadec-12-ene-9-sulfonyl)-4-methyl-benzene
88338-60-7

1-((Z)-9-Isocyano-nonadec-12-ene-9-sulfonyl)-4-methyl-benzene

Conditions
ConditionsYield
Multi-step reaction with 3 steps
1: triethylamine / CH2Cl2
2: 0.9 g / NaI / acetone / 3 h
3: 0.31 g / NaH / dimethylsulfoxide; diethyl ether / 3 h / Ambient temperature
View Scheme
(Z)-dec-3-en-1-ol
10340-22-4

(Z)-dec-3-en-1-ol

1-((Z)-10-Isocyano-icos-13-ene-10-sulfonyl)-4-methyl-benzene
88338-61-8

1-((Z)-10-Isocyano-icos-13-ene-10-sulfonyl)-4-methyl-benzene

Conditions
ConditionsYield
Multi-step reaction with 3 steps
1: triethylamine / CH2Cl2
2: 0.9 g / NaI / acetone / 3 h
3: 0.180 g / NaH / dimethylsulfoxide; diethyl ether
View Scheme
(Z)-dec-3-en-1-ol
10340-22-4

(Z)-dec-3-en-1-ol

(Z)-dodeca-1,5-dien-3-one
1537890-32-6

(Z)-dodeca-1,5-dien-3-one

Conditions
ConditionsYield
Multi-step reaction with 3 steps
1: Dess-Martin periodane / dichloromethane / 3 h / 20 °C
2: tetrahydrofuran / 0 - 20 °C
3: Dess-Martin periodane / dichloromethane / 3 h / 20 °C
View Scheme
Multi-step reaction with 3 steps
1: Dess-Martin periodane / dichloromethane / 3 h / 20 °C
2: tetrahydrofuran / 0 - 20 °C
3: Dess-Martin periodane / dichloromethane / 3 h / 20 °C
View Scheme
(Z)-dec-3-en-1-ol
10340-22-4

(Z)-dec-3-en-1-ol

(Z)-dodeca-1,5-dien-3-ol
123810-98-0

(Z)-dodeca-1,5-dien-3-ol

Conditions
ConditionsYield
Multi-step reaction with 2 steps
1: Dess-Martin periodane / dichloromethane / 3 h / 20 °C
2: tetrahydrofuran / 0 - 20 °C
View Scheme
(Z)-dec-3-en-1-ol
10340-22-4

(Z)-dec-3-en-1-ol

A

C10H20O2

C10H20O2

B

C10H20O2

C10H20O2

Conditions
ConditionsYield
With titanium(IV) isopropylate; tert.-butylhydroperoxide; 3,3'-bis(7-tert-butyl-8-hydroxyquinolin-2-yl)-1,1'-binaphthyl-2,2'-diol In dichloromethane; water at 20℃; for 48h; Inert atmosphere; Overall yield = 64 %; Optical yield = 85 %ee; enantioselective reaction;A n/a
B n/a
(Z)-dec-3-en-1-ol
10340-22-4

(Z)-dec-3-en-1-ol

3-bromopropyl (Z)-dec-3-enoate

3-bromopropyl (Z)-dec-3-enoate

Conditions
ConditionsYield
Multi-step reaction with 2 steps
1: potassium dichromate; sodium periodate; nitric acid / water; acetonitrile / 12 h / 0 - 20 °C
2: dmap; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride / dichloromethane / 12 h / 20 °C
View Scheme
(Z)-dec-3-en-1-ol
10340-22-4

(Z)-dec-3-en-1-ol

(Z)-trideca-1,2,6-triene

(Z)-trideca-1,2,6-triene

Conditions
ConditionsYield
Multi-step reaction with 4 steps
1: triethylamine / dichloromethane / 0 °C
2: lithium bromide / acetone / 3 h / Reflux
3: dimethyl sulfoxide / 12 h / 0 - 23 °C
4: copper(l) iodide; N-cyclohexyl-cyclohexanamine / 1,4-dioxane / 8 h / 100 °C
View Scheme
(Z)-dec-3-en-1-ol
10340-22-4

(Z)-dec-3-en-1-ol

2-((5Z,9Z,13Z)-icosa-5,9,13-trien-1-yloxy)tetrahydro-2H-pyran

2-((5Z,9Z,13Z)-icosa-5,9,13-trien-1-yloxy)tetrahydro-2H-pyran

Conditions
ConditionsYield
Multi-step reaction with 5 steps
1: triethylamine / dichloromethane / 0 °C
2: lithium bromide / acetone / 3 h / Reflux
3: dimethyl sulfoxide / 12 h / 0 - 23 °C
4: copper(l) iodide; N-cyclohexyl-cyclohexanamine / 1,4-dioxane / 8 h / 100 °C
5: ethylmagnesium bromide; bis(cyclopentadienyl)titanium dichloride; magnesium / diethyl ether / 6 h / 0 - 22 °C / Inert atmosphere
View Scheme
(Z)-dec-3-en-1-ol
10340-22-4

(Z)-dec-3-en-1-ol

(5Z,9Z,13Z)-icosa-5,9,13-trienoic acid

(5Z,9Z,13Z)-icosa-5,9,13-trienoic acid

Conditions
ConditionsYield
Multi-step reaction with 6 steps
1: triethylamine / dichloromethane / 0 °C
2: lithium bromide / acetone / 3 h / Reflux
3: dimethyl sulfoxide / 12 h / 0 - 23 °C
4: copper(l) iodide; N-cyclohexyl-cyclohexanamine / 1,4-dioxane / 8 h / 100 °C
5: ethylmagnesium bromide; bis(cyclopentadienyl)titanium dichloride; magnesium / diethyl ether / 6 h / 0 - 22 °C / Inert atmosphere
6: Jones reagent / dichloromethane; acetone / 1 h / 20 - 22 °C
View Scheme

10340-22-4Relevant articles and documents

Structure-Odor Relationships of (Z)-3-Alken-1-ols, (Z)-3-Alkenals, and (Z)-3-Alkenoic Acids

Lorber, Katja,Zeh, Gina,Regler, Johanna,Buettner, Andrea

, p. 2334 - 2343 (2018)

(Z)-3-Unsaturated volatile acids, alcohols, and aldehydes are commonly found in foods and other natural sources, playing a vital role in the attractiveness of foods but also as compounds with chemocommunicative function in entomology. However, a systematic investigation of their smell properties, especially regarding humans, has not been carried out until today. To close this gap, the odor thresholds in air and odor qualities of homologous series of (Z)-3-alken-1-ols, (Z)-3-alkenals, and (Z)-3-alkenoic acids were determined by gas chromatography-olfactometry. It was found that the odor qualities in the series of the (Z)-3-alken-1-ols and (Z)-3-alkenals changed, with increasing chain length, from grassy, green to an overall fatty and citrus-like, soapy character. On the other hand, the odor qualities of the (Z)-3-alkenoic acids changed successively from cheesy, sweaty via plastic-like, to waxy in their homologous series. With regard to their odor potencies, the lowest thresholds in air were found for (Z)-3-hexenal, (Z)-3-octenoic acid, and (Z)-3-octenal.

Isolation and identification of sex pheromone of Symmetrischema tangolias (Gyen) (Lepidoptera: Gelechiidae)

Griepink,Van Beek,Visser,Voerman,De Groot

, p. 2003 - 2013 (1995)

-

NbCl5-Mg reagent system in regio-and stereoselective synthesis of (2Z)-alkenylamines and (3Z)-alkenylols from substituted 2-alkynylamines and 3-alkynylols

Dzhemilev, Usein M.,Gabdullin, Azat M.,Kadikova, Rita N.,Mozgovoj, Oleg S.,Ramazanov, Ilfir R.

supporting information, (2021/07/02)

The reduction of N,N-disubstituted 2-alkynylamines and substituted 3-alkynylols using the NbCl5 –Mg reagent system affords the corresponding dideuterated (2Z)-alkenylamine and (3Z)-alkenylol derivatives in high yields in a regio-and stereoselective manner through the deuterolysis (or hydrolysis). The reaction of substituted propargylamines and homopropargylic alcohols with the in situ generated low-valent niobium complex (based on the reaction of NbCl5 with magnesium metal) is an efficient tool for the synthesis of allylamines and homoallylic alcohols bearing a 1,2-disubstituted double bond. It was found that the well-known approach for the reduction of alkynes based on the use of the TaCl5-Mg reagent system does not work for 2-alkynylamines and 3-alkynylols. Thus, this article reveals a difference in the behavior of two reagent systems—NbCl5-Mg and TaCl5-Mg, in relation to oxygen-and nitrogen-containing alkynes. A regio-and stereoselective method was developed for the synthesis of nitrogen-containing E-β-chlorovinyl sulfides based on the reaction of 2-alkynylamines with three equivalents of methanesulfonyl chloride in the presence of stoichiometric amounts of niobium(V) chloride and magnesium metal in toluene.

COMPOUNDS AND COMPOSITIONS FOR INTRACELLULAR DELIVERY OF AGENTS

-

Paragraph 00956, (2019/01/08)

The disclosure features amino lipids and compositions involving the same. Nanoparticle compositions include an amino lipid as well as additional lipids such as phospholipids, structural lipids, PEG lipids, or a combination thereof. Nanoparticle compositions further including therapeutic and/or prophylactic agents such as RNA are useful in the delivery of therapeutic and/or prophylactic agents to mammalian cells or organs to, for example, regulate polypeptide, protein, or gene expression.

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1

What can I do for you?
Get Best Price

Get Best Price for 10340-22-4