CAS No.10340-22-4,(Z)-3-decenol Suppliers

Dayang Chem (Hangzhou) Co.,Ltd.

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(Z)-3-decen-1-ol

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Henan Tianfu Chemical Co., Ltd.

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3-Decen-1-ol, (3Z)- 10340-22-4

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Hangzhou J&H Chemical Co., Ltd.

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Siwei Development Group Ltd.

Product name: (Z)-Dec-3-en-1-ol CAS No.：10340-22-4 Molecule Formula：C10H20O Molecule Weight：156.27 Purity: 99.0% Package: 25kg/drum Description：White powder Manufacture Standards：Enterprise Standard TESTING ITEMS

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Henan Wentao Chemical Product Co., Ltd.

We are leading fine chemicals supplier in China with ISO certificate, Our main business covers the fields below: 1.Noble Metal Catalysts (Pt.Pd...) 2.Organic Phosphine Ligands (Tert-butyl-phosphine.Cyclohexyl-phosphine...) 3.OLED

(Z)-3-decenolCAS NO.: 10340-22-4

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TAIZHOU ZHENYU BIOTECHNOLOGY CO., LTD

Zhenyu biotech exported this product to many countries and regions at best price. if you are looking for the material's manufacturer or supplier in china, zhenyu biotech is your best choice. pls contact with us freely for getting detailed

(Z)-3-decenol

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Xi`an Eastling Biotech Co., Ltd.

high purity lowest priceAppearance:solid or liquid Storage:in sealed air resistant place Package:Foil bag; Drum; Plastic bottle Application:Pharma;Industry;Agricultural Transportation:by sea or air Port:Beijing or Guangzhou

(Z)-3-decenol

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3-Decen-1-ol, (3Z)-

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Hangzhou ZeErRui Chemical Co., Ltd.

Product name:(Z)-3-decenol Synonyms:(3Z)-3-Decen-1-ol;(Z)-3-Decen-1-ol;cis-Slaterol;3-Decen-1-ol, (3Z)-;3-Decen-1-ol, (Z)-;3-Dedecen-1-ol, (Z)- CAS No:10340-22-4 Molecular formula:C10H20O Molecular Weight:156.27 Appearance:White Powder Boiling

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3-DECEN-1-OL,(3Z)-Appearance:white crystalline powder Storage:Store in dry, dark and ventilated place Package:25KG drum Application:intermediate Transportation:by air, by sea, by express

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(Z)-3-decenol CAS NO.10340-22-4

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Synthetic route

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

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

Conditions

Conditions	Yield
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%

: 137103-87-8
(Z)-1-(2-tetrahydropyranyloxy)-dec-3-ene

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

Conditions

Conditions	Yield
With toluene-4-sulfonic acid In methanol for 6h; Ambient temperature;	82%

: 1191-99-7
2,3-dihydro-2H-furan

: 3761-92-0
n-hexylmagnesium bromide

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

Conditions

Conditions	Yield
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%

: 111-71-7
heptanal

: 51860-45-8
3-hydroxypropyltriphenylphosphonium bromide

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

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

Conditions

Conditions	Yield
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;

...Expand

: 138041-89-1
1,4-decadien-3-ol

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

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

Conditions

Conditions	Yield
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;

: 629-05-0
n-octyne

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

Conditions

Conditions	Yield
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

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

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

Conditions

Conditions	Yield
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℃;

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

: 124-63-0
methanesulfonyl chloride

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

Conditions

Conditions	Yield
With triethylamine In dichloromethane
With triethylamine In dichloromethane at 0℃;

: 6975-99-1
6-dodecyne

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

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

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

Conditions

Conditions	Yield
Yield given. Multistep reaction. Yields of byproduct given. Title compound not separated from byproducts;

...Expand

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

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

Conditions

Conditions	Yield
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

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

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

Conditions

Conditions	Yield
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;

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

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

Conditions

Conditions	Yield
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

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

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

Conditions

Conditions	Yield
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

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

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

Conditions

Conditions	Yield
Multi-step reaction with 3 steps 1: CBr4; Ph3P / tetrahydrofuran 2: tetrahydrofuran; hexamethylphosphoric acid triamide 3: n-BuLi / hexamethylphosphoric acid triamide View Scheme

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

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

Conditions

Conditions	Yield
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

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

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

Conditions

Conditions	Yield
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

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

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

Conditions

Conditions	Yield
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

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

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

Conditions

Conditions	Yield
Multi-step reaction with 2 steps 1: triethylamine / CH2Cl2 2: 0.9 g / NaI / acetone / 3 h View Scheme

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

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

Conditions

Conditions	Yield
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

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

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

Conditions

Conditions	Yield
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

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

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

Conditions

Conditions	Yield
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

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

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

Conditions

Conditions	Yield
Multi-step reaction with 2 steps 1: Dess-Martin periodane / dichloromethane / 3 h / 20 °C 2: tetrahydrofuran / 0 - 20 °C View Scheme

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

A: C10H20O2

B: C10H20O2

Conditions

Conditions	Yield
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

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

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

Conditions

Conditions	Yield
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

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

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

Conditions

Conditions	Yield
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

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

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

Conditions

Conditions	Yield
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

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

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

Conditions

Conditions	Yield
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

Yield

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

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TAIZHOU ZHENYU BIOTECHNOLOGY CO., LTD

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Antimex Chemical Limied

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Hangzhou Fandachem Co.,Ltd

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U-Chemo Holding Co.,Limited

Shanghai Run-Biotech Co., Ltd.

Shanghai Ingredients Technology Co., Ltd.

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