DayangChem exported this product to many countries and regions at best price. If you are looking for the material's manufacturer or supplier in China, DayangChem is your best choice. Pls contact with us freely for getting detailed product spe
Cas:1070-65-1
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inquiryThe above product is Ality Chemical's strong item with best price, good quality and fast supply. Ality Chemical has been focusing on the research and production of this field for over 14 years. At the same time, we are always committed to providi
Cas:1070-65-1
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inquiryOur main production base is located in Xuzhou industry park. We are certified both to the ISO 9001 and ISO 14001 Standards, have a safety management system in place.Our R&D team masters core technology for process-design of target building block
Cas:1070-65-1
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FOB Price: $1.2 / 5.0
Type:Manufacturers
inquiryWITH US,YOUR MONEY IN SAFE,YOUR BUSINESS IN SAFE 1)Quick Response Within 12 hours; 2)Quality Guarantee: All products are strictly tested by our QC, confirmed by QA and approved by third party lab in China, USA, Canada, Germany, UK, Italy, France et
Cas:1070-65-1
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inquiryOur Advantage Rich Experience Our products are sold all over Europe,North&South America, Sino-East, Asia and pacific area as well as Africa,we establish long term. Quality service Company cooperates with research institutes. We strictly con
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FOB Price: $1.0 / 10.0
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inquiry1.In No Less 10 years exporting experience. you can 100% received goods 2.Lower Price with higher quality 3,Free sample 4,We are sincerely responsible for the "product quality" and "After Service" Upbio is Specializ
Cas:1070-65-1
Min.Order:1 Gram
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inquiryHenan Wentao Chemical Product Co.,Ltd is Located in Zhengzhou High-tech Development Zone with import and export license, We passed ISO 9001:2008 as well, Henan Wentao has developed more than 1000 compounds, which are widely used in the fields of prod
Cas:1070-65-1
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inquiryJ&H CHEM R&D center can offer custom synthesis according to the contract research and development services for the fine chemicals, pharmaceutical, biotechnique and some of the other chemicals. J&H CHEM has some Manufacturing base in Jia
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inquiryZibo Hangyu Biotechnology Development Co., Ltd is a leading manufacturer and supplier of chemicals in China. We develop produce and distribute high quality pharmaceuticals, intermediates, special chemicals and OLED intermediates and other fine chemi
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Min.Order:10 Gram
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inquiryZhenyu 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
Cas:1070-65-1
Min.Order:1 Kilogram
FOB Price: $2.0
Type:Lab/Research institutions
inquiryTAIHO Unique Advantages:1.We're factory2.Free samples available3.Commodity inspection can be done4.ISO9001,Kosher certifications5.10 years experiences Storage:Store in cool &dry place Package:aluminium foil bag/fiber can/plastic drum Application:comp
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
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inquiryIndependent research and development of impurities, familiar with the market and impurity characteristics; We can ship out on the same day if the products are in stock; Focus on impurity development of new products in the market; Expert in customizi
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inquiry1. Product advantages? High purity, all above 98.5%, no impurities after dissolution? We will test each batch to ensure quality? OEM and private brand services designed for free? Various cap colors available? We can also provide MT1 peptide powder2.
factory?direct?sale Application:healing drugs
Cas:1070-65-1
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inquiryWe are committed to providing our customers with the best products and services at the most competitive prices.Appearance:white crystalline powder Storage:Room temperature with sealed well Package:according to the clients requirement Application:Use
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inquiryETHYL 8-CHLORO-6-HYDROXYOCTANATEAppearance:white crystalline powder Storage:Store in dry, dark and ventilated place Package:25KG drum Application:pharmaceutical intermediate Transportation:by air, by sea, by express
factory?direct?saleAppearance:White powder Storage:Sealed and preserved Package:200/Kilograms Application:healing drugs Transportation:By sea Port:Shanghai/tianjin
Cas:1070-65-1
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Negotiable
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inquiry1070-65-1 Application:intermediate
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inquiryGood Quality Package:1kg/bag Application:Medical or chemical Transportation:Air/Train/Sea Port:Shenzhen
The factory supplies Application:manufacturing supplies
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inquiryfactory?direct?sale Application:Fine chemical intermediates, used as the main raw material for the synthesis of various pesticides, medicines, surfactants, polymer monomers, and antifungal agents
Cas:1070-65-1
Min.Order:0
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Type:Other
inquiryfactory?direct?saleAppearance:White powder Storage:Sealed and preserved Package:200/Kilograms Application:healing drugs Transportation:By sea Port:Shanghai/tianjin
Henan Sunlake Enterprise Corporation Our Advantages 1, Any inquiry about ch
Cas:1070-65-1
Min.Order:1 Kilogram
Negotiable
Type:Trading Company
inquiryShanghai, Run-Biotech Co., Ltd is a leading domestic pharmaceutical, biopharmaceutical, and health care products R & D outsourcing services company. As an innovation-driven and customer-focused company, Run Biotech provides a broad and integrated por
FINETECH INDUSTRY LIMITED is a LONDON based CRO company providing drug discovery & development services to worldwide clients. FINETECH INDUSTRY LIMITED supplies the ETHYL 8-CHLORO-6-HYDROXYOCTANATE, CAS:1070-65-1 with the most competitive price and t
Topbatt Chemical Co., Ltd., Established in 2019, located in Shenzhen, Guangdong Province, is a Manufacturer and Trading company which specialized in fine chemicals like Pharmaceutical Reference Standards and Stable Isotopes. Our Stable Isotopes produ
Cas:1070-65-1
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Type:Lab/Research institutions
inquiryDebyesci is here who supplied several kinds of chemical products to global pharmaceutical, drug discovery, agrochemical and biotechnology industries for four yearsOur key scientific leadership team has gained experience in top research and developmen
Cas:1070-65-1
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Type:Lab/Research institutions
inquiry1. Our staff are all biomedical related majors with rich experience in the pharmaceutical industry, and can provide you with more professional services.2. Our supplier has a good quality management system, and the quality of products is reliable and
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; |
6-hydroxy-8-chlorooctanoic acid ethyl ester
Conditions | Yield |
---|---|
With sodium tetrahydroborate; tetrabutylammomium bromide; ammonia In 1,2-dichloro-ethane at 10 - 30℃; for 2h; Large scale; | 95 kg |
6-hydroxy-8-chlorooctanoic acid ethyl ester
6,8-dichlorooctanoic acid ethyl ester
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 |
6-hydroxy-8-chlorooctanoic acid ethyl ester
(+)-8-chloro-6-hydroxy-octanoic acid
Conditions | Yield |
---|---|
With lithium hydroxide In ethanol Ambient temperature; Yield given; |
6-hydroxy-8-chlorooctanoic acid ethyl ester
N-(3-chloropropyl)-8-chloro-6-hydroxyoctylamine
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 |
6-hydroxy-8-chlorooctanoic acid ethyl ester
N-(3-chloropropyl)-8-chloro-6-hydroxyoctanamide
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 |
6-hydroxy-8-chlorooctanoic acid ethyl ester
N-(tert-butyloxycarbonyl)-N-(3-chloropropyl)-8-chloro-6-hydroxyoctylamine
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 |
6-hydroxy-8-chlorooctanoic acid ethyl ester
(8-Chloro-6-hydroxy-octyl)-(3-chloro-propyl)-carbamic acid benzyl ester
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 |
6-hydroxy-8-chlorooctanoic acid ethyl ester
N-(tert-butyloxycarbonyl)-N-(3-azidopropyl)-8-azido-6-hydroxyoctylamine
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 |
6-hydroxy-8-chlorooctanoic acid ethyl ester
(8-Chloro-6-hydroxy-octyl)-(3-chloro-propyl)-carbamic acid 4-nitro-benzyl ester
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 |
6-hydroxy-8-chlorooctanoic acid ethyl ester
(8-Azido-6-hydroxy-octyl)-(3-azido-propyl)-carbamic acid benzyl ester
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 |
6-hydroxy-8-chlorooctanoic acid ethyl ester
Methanesulfonic acid 1-(2-azido-ethyl)-6-[(3-azido-propyl)-tert-butoxycarbonyl-amino]-hexyl ester
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 |
6-hydroxy-8-chlorooctanoic acid ethyl ester
(8-Azido-6-hydroxy-octyl)-(3-azido-propyl)-carbamic acid 4-nitro-benzyl ester
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 |
6-hydroxy-8-chlorooctanoic acid ethyl ester
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 |
6-hydroxy-8-chlorooctanoic acid ethyl ester
Methanesulfonic acid 1-(2-azido-ethyl)-6-[(3-azido-propyl)-benzyloxycarbonyl-amino]-hexyl ester
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 |
6-hydroxy-8-chlorooctanoic acid ethyl ester
Methanesulfonic acid 1-(2-azido-ethyl)-6-[(3-azido-propyl)-(4-nitro-benzyloxycarbonyl)-amino]-hexyl ester
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 |
6-hydroxy-8-chlorooctanoic acid ethyl ester
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 |
6-hydroxy-8-chlorooctanoic acid ethyl ester
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 |
6-hydroxy-8-chlorooctanoic acid ethyl ester
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 |
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 4-nitro-benzyl ester
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 |
vinyl propionate
6-hydroxy-8-chlorooctanoic acid ethyl ester
B
ethyl (R)-8-chloro-6-hydroxyoctanoate
C
acetaldehyde
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 |
vinyl n-butyrate
6-hydroxy-8-chlorooctanoic acid ethyl ester
B
ethyl (R)-8-chloro-6-hydroxyoctanoate
C
acetaldehyde
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 |
6-hydroxy-8-chlorooctanoic acid ethyl ester
acetic anhydride
B
ethyl (R)-8-chloro-6-hydroxyoctanoate
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 |
butanoic acid anhydride
6-hydroxy-8-chlorooctanoic acid ethyl ester
B
ethyl (R)-8-chloro-6-hydroxyoctanoate
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 |
6-hydroxy-8-chlorooctanoic acid ethyl ester
2-Methylpropionic anhydride
B
ethyl (R)-8-chloro-6-hydroxyoctanoate
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 |
pentanoic anhydride
6-hydroxy-8-chlorooctanoic acid ethyl ester
B
ethyl (R)-8-chloro-6-hydroxyoctanoate
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 |
vinyl acetate
6-hydroxy-8-chlorooctanoic acid ethyl ester
B
ethyl (R)-8-chloro-6-hydroxyoctanoate
C
acetaldehyde
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 |
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