90435-60-2

Basic information

• Product Name: (+)-8-chloro-6-hydroxy-octanoic acid
• Synonyms: (+)-8-chloro-6-hydroxy-octanoic acid
• CAS NO: 90435-60-2
• Molecular Weight: 194.658
• Mol File: 90435-60-2.mol
• Article Data: 0

Chemical Properties

• Melting Point: 51-53 °C(Solv: benzene (71-43-2); ligroine (8032-32-4))
• Boiling Point: 160-165 °C(Press: 0.5 Torr)
• Density: 1.183±0.06 g/cm3(Predicted)
• CAS DataBase Reference: (+)-8-chloro-6-hydroxy-octanoic acid(CAS DataBase Reference)
• NIST Chemistry Reference: (+)-8-chloro-6-hydroxy-octanoic acid(90435-60-2)
• EPA Substance Registry System: (+)-8-chloro-6-hydroxy-octanoic acid(90435-60-2)

Safety Data

• Hazardous Substances Data: 90435-60-2(Hazardous Substances Data)

Usage

Description

(+)-8-chloro-6-hydroxy-octanoic acid is a chiral chemical compound with the molecular formula C8H15ClO3. It is a derivative of octanoic acid, a fatty acid commonly found in coconut oil and palm kernel oil. The addition of a hydroxyl group and a chlorine atom to the octanoic acid molecule gives rise to this unique compound. Its chiral nature, with a non-superimposable mirror image, makes it a valuable tool for studying chiral interactions and synthesizing other chiral compounds.

Uses

Used in Pharmaceutical Industry:
(+)-8-chloro-6-hydroxy-octanoic acid is used as a potential candidate for the development of new drugs due to its unique chemical structure. Its chiral properties and ability to interact with other chiral molecules make it a promising compound for pharmaceutical research and drug discovery.
Used in Biotechnology:
(+)-8-chloro-6-hydroxy-octanoic acid is used as a valuable tool in biotechnology for studying chiral interactions and developing new methods for synthesizing chiral compounds. Its unique structure and properties can contribute to advancements in the field of biotechnology.
Used in Organic Chemistry:
(+)-8-chloro-6-hydroxy-octanoic acid is used as a versatile building block in organic chemistry for the synthesis of other chiral compounds. Its unique structure allows for various chemical reactions and modifications, making it a valuable resource for organic chemists.

Downstream Products

• 120476-75-7 (8-Chloro-6-hydroxy-octyl)-(3-chloro-propyl)-carbamic acid benzyl ester 
• 120476-76-8 (8-Chloro-6-hydroxy-octyl)-(3-chloro-propyl)-carbamic acid 4-nitro-benzyl ester 
• 120476-77-9 (8-Azido-6-hydroxy-octyl)-(3-azido-propyl)-carbamic acid benzyl ester 
• 120476-78-0 (8-Azido-6-hydroxy-octyl)-(3-azido-propyl)-carbamic acid 4-nitro-benzyl ester 
• 120496-27-7 Methanesulfonic acid 1-(2-azido-ethyl)-6-[(3-azido-propyl)-benzyloxycarbonyl-amino]-hexyl ester 
• 120476-80-4 Methanesulfonic acid 1-(2-azido-ethyl)-6-[(3-azido-propyl)-(4-nitro-benzyloxycarbonyl)-amino]-hexyl 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 
• 41443-60-1 (+)-6,8-dichloro-octanoic acid