1070-65-1

• 

• Basic information

  1. Product Name: ETHYL 8-CHLORO-6-HYDROXYOCTANATE
  2. Synonyms: 6-HYDROXY-8-CHLORO OCTANOIC ACID ETHYL ESTER;ETHYL 8-CHLORO-6-HYDROXYOCTANATE;Octanoic acid, 8-chloro-6-hydroxy-, ethyl ester
  3. CAS NO:1070-65-1
  4. Molecular Formula: C₁₀H₁₉ClO₃
  5. Molecular Weight: 222.71
  6. EINECS: N/A
  7. Product Categories: Pharmaceutical Intermediates;Organic acids
  8. Mol File: 1070-65-1.mol
  9. Article Data: 1

• Chemical Properties

  1. Melting Point: N/A
  2. Boiling Point: 311.2 °C at 760 mmHg
  3. Flash Point: 142 °C
  4. Appearance: /
  5. Density: 1.079 g/cm³
  6. Vapor Pressure: 5.08E-05mmHg at 25°C
  7. Refractive Index: 1.459
  8. Storage Temp.: N/A
  9. Solubility: N/A
  10. PKA: 14.71±0.20(Predicted)
  11. CAS DataBase Reference: ETHYL 8-CHLORO-6-HYDROXYOCTANATE(CAS DataBase Reference)
  12. NIST Chemistry Reference: ETHYL 8-CHLORO-6-HYDROXYOCTANATE(1070-65-1)
  13. EPA Substance Registry System: ETHYL 8-CHLORO-6-HYDROXYOCTANATE(1070-65-1)

• Safety Data

  1. Hazard Codes: N/A
  2. Statements: N/A
  3. Safety Statements: N/A
  4. WGK Germany:
  5. RTECS:
  6. HazardClass: N/A
  7. PackingGroup: N/A
  8. Hazardous Substances Data: 1070-65-1(Hazardous Substances Data)

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• Usage
• SDS
• Synthetic route
• Upstream product
• Downstream Products
• Article

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• Ethyl 8-chloro-6-hydroxyoctanate

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• Factory Supply ETHYL 8-CHLORO-6-HYDROXYOCTANATE

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• 8-Chloro-6-hydroxyoctanoic acid ethyl ester

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• Pharmaceutical Grade CAS 1070-65-1 with competitive price

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• ETHYL 8-CHLORO-6-HYDROXYOCTANATE CAS:1070-65-1

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• Octanoic acid,8-chloro-6-hydroxy-, ethyl ester

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• Octanoic acid,8-chloro-6-hydroxy-, ethyl ester

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• Ethyl8-chloro-6-hydroxyoctanate

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• Hangzhou J&H Chemical Co., Ltd.
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• Octanoic acid,8-chloro-6-hydroxy-, ethyl ester

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• ETHYL 8-CHLORO-6-HYDROXYOCTANATE

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1070-65-1 Usage

Uses

Ethyl 8-chloro-6-hydroxyoctanoate is used in biological study for the enzymic resolution of chiral chlorohydrin precursor for (R)-α-lipoic acid synthesis via lipase catalyzed enantioselective transacylation with vinyl acetate.

Check Digit Verification of cas no

The CAS Registry Mumber 1070-65-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,0,7 and 0 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1070-65:
(6*1)+(5*0)+(4*7)+(3*0)+(2*6)+(1*5)=51
51 % 10 = 1
So 1070-65-1 is a valid CAS Registry Number.

InChI:InChI=1/C10H19ClO3/c1-2-14-10(13)6-4-3-5-9(12)7-8-11/h9,12H,2-8H2,1H3

1070-65-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name	ethyl 8-chloro-6-hydroxyoctanoate

1.2 Other means of identification

Product number	-
Other names	ETHYL 8-CHLORO-6-HYDROXYOCTANATE

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:1070-65-1 SDS

1070-65-1Synthetic route

626-86-8

adipinic acid monoethyl ester

1070-65-1

6-hydroxy-8-chlorooctanoic acid ethyl ester

Conditions

Conditions	Yield
With thionyl chloride; 1,1,2,2-tetrachloroethane anschliessendes Behandeln mit Aethylen und Aluminiumchlorid und Behandeln der nach dem Versetzen mit wss.Salzsaeure erhaltenen nicht-waessrigen Phase des Reaktionsgemisches mit Natriumboranat in Aethanol;

ethyl 6-oxo-8-chlorooctanoate

1070-65-1

6-hydroxy-8-chlorooctanoic acid ethyl ester

Conditions

Conditions	Yield
With sodium tetrahydroborate; tetrabutylammomium bromide; ammonia In 1,2-dichloro-ethane at 10 - 30℃; for 2h; Large scale;	95 kg

1070-65-1

6-hydroxy-8-chlorooctanoic acid ethyl ester

1070-64-0

6,8-dichlorooctanoic acid ethyl ester

Conditions

Conditions	Yield
With phosgene; N,N'-dimethylbenzylamine In 1,2-dichloro-ethane at 10 - 75℃; for 2.5h; Concentration; Solvent; Reagent/catalyst; Temperature;	96.69%
With pyridine; thionyl chloride; benzene
With thionyl chloride In toluene at 100℃; for 5h; Reagent/catalyst; Solvent; Cooling with ice; Large scale;	480 kg

1070-65-1

6-hydroxy-8-chlorooctanoic acid ethyl ester

90435-60-2

(+)-8-chloro-6-hydroxy-octanoic acid

Conditions

Conditions	Yield
With lithium hydroxide In ethanol Ambient temperature; Yield given;

1070-65-1

6-hydroxy-8-chlorooctanoic acid ethyl ester

120476-67-7

N-(3-chloropropyl)-8-chloro-6-hydroxyoctylamine

Conditions

Conditions	Yield
Multi-step reaction with 3 steps 1: LiOH*H2O / aq. ethanol / Ambient temperature 2: 89 percent / N-methylmorpholine, 1-N-hydroxybenzotriazole, dicyclohexylcarbodiimide / dimethylformamide / 96 h / Ambient temperature 3: 75.4 percent / B2H6 / tetrahydrofuran / Ambient temperature View Scheme

1070-65-1

6-hydroxy-8-chlorooctanoic acid ethyl ester

120476-66-6

N-(3-chloropropyl)-8-chloro-6-hydroxyoctanamide

Conditions

Conditions	Yield
Multi-step reaction with 2 steps 1: LiOH*H2O / aq. ethanol / Ambient temperature 2: 89 percent / N-methylmorpholine, 1-N-hydroxybenzotriazole, dicyclohexylcarbodiimide / dimethylformamide / 96 h / Ambient temperature View Scheme

1070-65-1

6-hydroxy-8-chlorooctanoic acid ethyl ester

120476-68-8

N-(tert-butyloxycarbonyl)-N-(3-chloropropyl)-8-chloro-6-hydroxyoctylamine

Conditions

Conditions	Yield
Multi-step reaction with 4 steps 1: LiOH*H2O / aq. ethanol / Ambient temperature 2: 89 percent / N-methylmorpholine, 1-N-hydroxybenzotriazole, dicyclohexylcarbodiimide / dimethylformamide / 96 h / Ambient temperature 3: 75.4 percent / B2H6 / tetrahydrofuran / Ambient temperature 4: 77 percent / NaHCO3, NaCl / CHCl3; H2O / 2 h / Heating View Scheme

1070-65-1

6-hydroxy-8-chlorooctanoic acid ethyl ester

120476-75-7

(8-Chloro-6-hydroxy-octyl)-(3-chloro-propyl)-carbamic acid benzyl ester

Conditions

Conditions	Yield
Multi-step reaction with 4 steps 1: LiOH*H2O / aq. ethanol / Ambient temperature 2: 89 percent / N-methylmorpholine, 1-N-hydroxybenzotriazole, dicyclohexylcarbodiimide / dimethylformamide / 96 h / Ambient temperature 3: 75.4 percent / B2H6 / tetrahydrofuran / Ambient temperature 4: 84 percent / 1M KOH / diethyl ether / Ambient temperature View Scheme

1070-65-1

6-hydroxy-8-chlorooctanoic acid ethyl ester

120476-69-9

N-(tert-butyloxycarbonyl)-N-(3-azidopropyl)-8-azido-6-hydroxyoctylamine

Conditions

Conditions

Yield

Multi-step reaction with 5 steps 1: LiOH*H2O / aq. ethanol / Ambient temperature 2: 89 percent / N-methylmorpholine, 1-N-hydroxybenzotriazole, dicyclohexylcarbodiimide / dimethylformamide / 96 h / Ambient temperature 3: 75.4 percent / B2H6 / tetrahydrofuran / Ambient temperature 4: 77 percent / NaHCO3, NaCl / CHCl3; H2O / 2 h / Heating 5: 93 percent / LiN3, LiI / dimethylformamide / 30 h / 60 °C View Scheme

1070-65-1

6-hydroxy-8-chlorooctanoic acid ethyl ester

120476-76-8

(8-Chloro-6-hydroxy-octyl)-(3-chloro-propyl)-carbamic acid 4-nitro-benzyl ester

Conditions

Conditions	Yield
Multi-step reaction with 4 steps 1: LiOH*H2O / aq. ethanol / Ambient temperature 2: 89 percent / N-methylmorpholine, 1-N-hydroxybenzotriazole, dicyclohexylcarbodiimide / dimethylformamide / 96 h / Ambient temperature 3: 75.4 percent / B2H6 / tetrahydrofuran / Ambient temperature 4: 70 percent / 1M KOH / diethyl ether / Ambient temperature View Scheme

1070-65-1

6-hydroxy-8-chlorooctanoic acid ethyl ester

120476-77-9

(8-Azido-6-hydroxy-octyl)-(3-azido-propyl)-carbamic acid benzyl ester

Conditions

Conditions

Yield

Multi-step reaction with 5 steps 1: LiOH*H2O / aq. ethanol / Ambient temperature 2: 89 percent / N-methylmorpholine, 1-N-hydroxybenzotriazole, dicyclohexylcarbodiimide / dimethylformamide / 96 h / Ambient temperature 3: 75.4 percent / B2H6 / tetrahydrofuran / Ambient temperature 4: 84 percent / 1M KOH / diethyl ether / Ambient temperature 5: 65 percent / LiN3, LiI / dimethylformamide / 30 h / 60 °C View Scheme

1070-65-1

6-hydroxy-8-chlorooctanoic acid ethyl ester

120476-79-1

Methanesulfonic acid 1-(2-azido-ethyl)-6-[(3-azido-propyl)-tert-butoxycarbonyl-amino]-hexyl ester

Conditions

Conditions

Yield

Multi-step reaction with 6 steps 1: LiOH*H2O / aq. ethanol / Ambient temperature 2: 89 percent / N-methylmorpholine, 1-N-hydroxybenzotriazole, dicyclohexylcarbodiimide / dimethylformamide / 96 h / Ambient temperature 3: 75.4 percent / B2H6 / tetrahydrofuran / Ambient temperature 4: 77 percent / NaHCO3, NaCl / CHCl3; H2O / 2 h / Heating 5: 93 percent / LiN3, LiI / dimethylformamide / 30 h / 60 °C 6: 92 percent / Et3N / CH2Cl2 / Ambient temperature View Scheme

1070-65-1

6-hydroxy-8-chlorooctanoic acid ethyl ester

120476-78-0

(8-Azido-6-hydroxy-octyl)-(3-azido-propyl)-carbamic acid 4-nitro-benzyl ester

Conditions

Conditions

Yield

Multi-step reaction with 5 steps 1: LiOH*H2O / aq. ethanol / Ambient temperature 2: 89 percent / N-methylmorpholine, 1-N-hydroxybenzotriazole, dicyclohexylcarbodiimide / dimethylformamide / 96 h / Ambient temperature 3: 75.4 percent / B2H6 / tetrahydrofuran / Ambient temperature 4: 70 percent / 1M KOH / diethyl ether / Ambient temperature 5: 88 percent / LiN3, LiI / dimethylformamide / 30 h / 60 °C View Scheme

1070-65-1

6-hydroxy-8-chlorooctanoic acid ethyl ester

N1-(3-Amino-propyl)-6-[(3aS,4S,6R,6aR)-6-(6-amino-purin-9-yl)-2,2-dimethyl-tetrahydro-furo[3,4-d][1,3]dioxol-4-ylmethylsulfanyl]-octane-1,8-diamine

Conditions

Conditions

Yield

Multi-step reaction with 8 steps 1: LiOH*H2O / aq. ethanol / Ambient temperature 2: 89 percent / N-methylmorpholine, 1-N-hydroxybenzotriazole, dicyclohexylcarbodiimide / dimethylformamide / 96 h / Ambient temperature 3: 75.4 percent / B2H6 / tetrahydrofuran / Ambient temperature 4: 70 percent / 1M KOH / diethyl ether / Ambient temperature 5: 88 percent / LiN3, LiI / dimethylformamide / 30 h / 60 °C 6: 99 percent / Et3N / CH2Cl2 / Ambient temperature 7: 43 percent / sodium methoxide / a) r.t., 48 h, b) 25 deg C, 12 h, sonication 8: 49 mg / H2, ethanol / 10percent Pd/C / methanol / 2585.7 Torr View Scheme

1070-65-1

6-hydroxy-8-chlorooctanoic acid ethyl ester

120496-27-7

Methanesulfonic acid 1-(2-azido-ethyl)-6-[(3-azido-propyl)-benzyloxycarbonyl-amino]-hexyl ester

Conditions

Conditions

Yield

Multi-step reaction with 6 steps 1: LiOH*H2O / aq. ethanol / Ambient temperature 2: 89 percent / N-methylmorpholine, 1-N-hydroxybenzotriazole, dicyclohexylcarbodiimide / dimethylformamide / 96 h / Ambient temperature 3: 75.4 percent / B2H6 / tetrahydrofuran / Ambient temperature 4: 84 percent / 1M KOH / diethyl ether / Ambient temperature 5: 65 percent / LiN3, LiI / dimethylformamide / 30 h / 60 °C 6: 88 percent / Et3N / CH2Cl2 / Ambient temperature View Scheme

1070-65-1

6-hydroxy-8-chlorooctanoic acid ethyl ester

120476-80-4

Methanesulfonic acid 1-(2-azido-ethyl)-6-[(3-azido-propyl)-(4-nitro-benzyloxycarbonyl)-amino]-hexyl ester

Conditions

Conditions

Yield

Multi-step reaction with 6 steps 1: LiOH*H2O / aq. ethanol / Ambient temperature 2: 89 percent / N-methylmorpholine, 1-N-hydroxybenzotriazole, dicyclohexylcarbodiimide / dimethylformamide / 96 h / Ambient temperature 3: 75.4 percent / B2H6 / tetrahydrofuran / Ambient temperature 4: 70 percent / 1M KOH / diethyl ether / Ambient temperature 5: 88 percent / LiN3, LiI / dimethylformamide / 30 h / 60 °C 6: 99 percent / Et3N / CH2Cl2 / Ambient temperature View Scheme

1070-65-1

6-hydroxy-8-chlorooctanoic acid ethyl ester

{6-[(3aS,4S,6R,6aR)-6-(6-Amino-purin-9-yl)-2,2-dimethyl-tetrahydro-furo[3,4-d][1,3]dioxol-4-ylmethylsulfanyl]-8-azido-octyl}-(3-azido-propyl)-carbamic acid tert-butyl ester

Conditions

Conditions

Yield

Multi-step reaction with 7 steps 1: LiOH*H2O / aq. ethanol / Ambient temperature 2: 89 percent / N-methylmorpholine, 1-N-hydroxybenzotriazole, dicyclohexylcarbodiimide / dimethylformamide / 96 h / Ambient temperature 3: 75.4 percent / B2H6 / tetrahydrofuran / Ambient temperature 4: 77 percent / NaHCO3, NaCl / CHCl3; H2O / 2 h / Heating 5: 93 percent / LiN3, LiI / dimethylformamide / 30 h / 60 °C 6: 92 percent / Et3N / CH2Cl2 / Ambient temperature 7: 28 percent / sodium methoxide / a) r.t., 48 h, b) 25 deg C, 12 h, sonication View Scheme

1070-65-1

6-hydroxy-8-chlorooctanoic acid ethyl ester

{6-[(3aS,4S,6R,6aR)-6-(6-Amino-purin-9-yl)-2,2-dimethyl-tetrahydro-furo[3,4-d][1,3]dioxol-4-ylmethylsulfanyl]-8-azido-octyl}-(3-azido-propyl)-carbamic acid benzyl ester

Conditions

Conditions

Yield

Multi-step reaction with 7 steps 1: LiOH*H2O / aq. ethanol / Ambient temperature 2: 89 percent / N-methylmorpholine, 1-N-hydroxybenzotriazole, dicyclohexylcarbodiimide / dimethylformamide / 96 h / Ambient temperature 3: 75.4 percent / B2H6 / tetrahydrofuran / Ambient temperature 4: 84 percent / 1M KOH / diethyl ether / Ambient temperature 5: 65 percent / LiN3, LiI / dimethylformamide / 30 h / 60 °C 6: 88 percent / Et3N / CH2Cl2 / Ambient temperature 7: 80 percent / sodium methoxide / a) r.t., 48 h, b) 25 deg C, 12 h, sonication View Scheme

1070-65-1

6-hydroxy-8-chlorooctanoic acid ethyl ester

S-(5'-deoxy-5'-adenosyl)-N-(3-aminopropyl)-8-amino-6-thiooctylamine formate salt

Conditions

Conditions

Yield

Multi-step reaction with 9 steps 1: LiOH*H2O / aq. ethanol / Ambient temperature 2: 89 percent / N-methylmorpholine, 1-N-hydroxybenzotriazole, dicyclohexylcarbodiimide / dimethylformamide / 96 h / Ambient temperature 3: 75.4 percent / B2H6 / tetrahydrofuran / Ambient temperature 4: 70 percent / 1M KOH / diethyl ether / Ambient temperature 5: 88 percent / LiN3, LiI / dimethylformamide / 30 h / 60 °C 6: 99 percent / Et3N / CH2Cl2 / Ambient temperature 7: 43 percent / sodium methoxide / a) r.t., 48 h, b) 25 deg C, 12 h, sonication 8: 49 mg / H2, ethanol / 10percent Pd/C / methanol / 2585.7 Torr 9: 88percent formic acid / 3 h / Ambient temperature View Scheme

1070-65-1

6-hydroxy-8-chlorooctanoic acid ethyl ester

120476-70-2

{6-[(3aS,4S,6R,6aR)-6-(6-Amino-purin-9-yl)-2,2-dimethyl-tetrahydro-furo[3,4-d][1,3]dioxol-4-ylmethylsulfanyl]-8-azido-octyl}-(3-azido-propyl)-carbamic acid 4-nitro-benzyl ester

Conditions

Conditions

Yield

Multi-step reaction with 7 steps 1: LiOH*H2O / aq. ethanol / Ambient temperature 2: 89 percent / N-methylmorpholine, 1-N-hydroxybenzotriazole, dicyclohexylcarbodiimide / dimethylformamide / 96 h / Ambient temperature 3: 75.4 percent / B2H6 / tetrahydrofuran / Ambient temperature 4: 70 percent / 1M KOH / diethyl ether / Ambient temperature 5: 88 percent / LiN3, LiI / dimethylformamide / 30 h / 60 °C 6: 99 percent / Et3N / CH2Cl2 / Ambient temperature 7: 43 percent / sodium methoxide / a) r.t., 48 h, b) 25 deg C, 12 h, sonication View Scheme

105-38-4

vinyl propionate

1070-65-1

6-hydroxy-8-chlorooctanoic acid ethyl ester

A

C13H23ClO4

B

852383-82-5

ethyl (R)-8-chloro-6-hydroxyoctanoate

C

75-07-0

acetaldehyde

Conditions

Conditions	Yield
With Novozym 435 (lipase B from Candida antarctica) In di-isopropyl ether at 40℃; for 7h; Resolution of racemate; Enzymatic reaction;	A n/a B n/a C n/a

123-20-6

vinyl n-butyrate

1070-65-1

6-hydroxy-8-chlorooctanoic acid ethyl ester

A

C14H25ClO4

B

852383-82-5

ethyl (R)-8-chloro-6-hydroxyoctanoate

C

75-07-0

acetaldehyde

Conditions

Conditions	Yield
With Novozym 435 (lipase B from Candida antarctica) In di-isopropyl ether at 40℃; for 7h; Resolution of racemate; Enzymatic reaction;	A n/a B n/a C n/a

1070-65-1

6-hydroxy-8-chlorooctanoic acid ethyl ester

108-24-7

acetic anhydride

A

C12H21ClO4

B

852383-82-5

ethyl (R)-8-chloro-6-hydroxyoctanoate

Conditions

Conditions	Yield
With Novozym 435 (lipase B from Candida antarctica) In di-isopropyl ether at 40℃; for 7h; Resolution of racemate; Enzymatic reaction;	A n/a B n/a

106-31-0

butanoic acid anhydride

1070-65-1

6-hydroxy-8-chlorooctanoic acid ethyl ester

A

C14H25ClO4

B

852383-82-5

ethyl (R)-8-chloro-6-hydroxyoctanoate

Conditions

Conditions	Yield
With Novozym 435 (lipase B from Candida antarctica) In di-isopropyl ether at 40℃; for 7h; Resolution of racemate; Enzymatic reaction;	A n/a B n/a

1070-65-1

6-hydroxy-8-chlorooctanoic acid ethyl ester

97-72-3

2-Methylpropionic anhydride

A

C14H25ClO4

B

852383-82-5

ethyl (R)-8-chloro-6-hydroxyoctanoate

Conditions

Conditions	Yield
With Novozym 435 (lipase B from Candida antarctica) In di-isopropyl ether at 40℃; for 7h; Resolution of racemate; Enzymatic reaction;	A n/a B n/a

2082-59-9

pentanoic anhydride

1070-65-1

6-hydroxy-8-chlorooctanoic acid ethyl ester

A

C15H27ClO4

B

852383-82-5

ethyl (R)-8-chloro-6-hydroxyoctanoate

Conditions

Conditions	Yield
With Novozym 435 (lipase B from Candida antarctica) In di-isopropyl ether at 40℃; for 7h; Resolution of racemate; Enzymatic reaction;	A n/a B n/a

108-05-4

vinyl acetate

1070-65-1

6-hydroxy-8-chlorooctanoic acid ethyl ester

A

C12H21ClO4

B

852383-82-5

ethyl (R)-8-chloro-6-hydroxyoctanoate

C

75-07-0

acetaldehyde

Conditions

Conditions	Yield
With Novozym 435 (lipase B from Candida antarctica) In di-isopropyl ether at 40℃; for 7h; Reagent/catalyst; Solvent; Time; Temperature; Resolution of racemate; Enzymatic reaction;	A n/a B n/a C n/a

1070-65-1Upstream product

• 626-86-8 adipinic acid monoethyl ester 

1070-65-1Downstream Products

• 1070-64-0 6,8-dichlorooctanoic acid ethyl ester 
• 852383-82-5 ethyl (R)-8-chloro-6-hydroxyoctanoate 
• 75-07-0 acetaldehyde 
• 120476-70-2 {6-[(3aS,4S,6R,6aR)-6-(6-Amino-purin-9-yl)-2,2-dimethyl-tetrahydro-furo[3,4-d][1,3]dioxol-4-ylmethylsulfanyl]-8-azido-octyl}-(3-azido-propyl)-carbamic acid 4-nitro-benzyl ester 
• 120476-80-4 Methanesulfonic acid 1-(2-azido-ethyl)-6-[(3-azido-propyl)-(4-nitro-benzyloxycarbonyl)-amino]-hexyl ester 
• 120496-27-7 Methanesulfonic acid 1-(2-azido-ethyl)-6-[(3-azido-propyl)-benzyloxycarbonyl-amino]-hexyl ester 
• 120476-78-0 (8-Azido-6-hydroxy-octyl)-(3-azido-propyl)-carbamic acid 4-nitro-benzyl ester 
• 120476-77-9 (8-Azido-6-hydroxy-octyl)-(3-azido-propyl)-carbamic acid benzyl ester 
• 120476-76-8 (8-Chloro-6-hydroxy-octyl)-(3-chloro-propyl)-carbamic acid 4-nitro-benzyl ester 
• 120476-75-7 (8-Chloro-6-hydroxy-octyl)-(3-chloro-propyl)-carbamic acid benzyl ester 

1070-65-1Relevant articles and documents

-

Reed,Niu

, p. 416,418 (1955)

-

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