61367-40-6

Basic information

• Product Name: H-D-CHG-OH HCL
• Synonyms: D-2-CYCLOHEXYLGLYCINE HYDROCHLORIDE;D-ALPHA-CYCLOHEXYLGLYCINE HYDROCHLORIDE SALT;D-CYCLOHEXYLGLYCINE HYDROCHLORIDE;H-D-CHG-OH HCL;H-D-PHG(HEXAHYDRO)-OH HCL;H-CYCLOHEXYL-D-GLY-OH HCL;D-ALPHA-Cyclohexylglycine hydrochloride;D--Cyclohexylglycine hydrochloride salt
• CAS NO: 61367-40-6
• Molecular Formula: C₈H₁₅NO₂*ClH
• Molecular Weight: 193.67
• Mol File: 61367-40-6.mol
• Article Data: 1

Chemical Properties

• Boiling Point: 322.7 °C at 760 mmHg
• Flash Point: 149 °C
• Appearance: white - off-white powder
• Vapor Pressure: 5.63E-05mmHg at 25°C
• Storage Temp.: Inert atmosphere,Room Temperature
• CAS DataBase Reference: H-D-CHG-OH HCL(CAS DataBase Reference)
• NIST Chemistry Reference: H-D-CHG-OH HCL(61367-40-6)
• EPA Substance Registry System: H-D-CHG-OH HCL(61367-40-6)

Safety Data

• Hazardous Substances Data: 61367-40-6(Hazardous Substances Data)

Usage

General Description

H-D-CHG-OH HCL is a chemical compound with the formula H-D-CHG-OH. H-D-CHG-OH HCL is a derivative of choline, a vital nutrient found in various foods such as eggs, liver, and soybeans. Choline is essential for several physiological processes, including the production of the neurotransmitter acetylcholine, as well as being a precursor for the synthesis of phospholipids. The addition of hydrochloric acid (HCL) to H-D-CHG-OH may be used to modify the compound for specific applications, potentially altering its solubility, stability, or reactivity in different chemical processes. H-D-CHG-OH HCL may have potential uses in pharmaceuticals, biochemical research, or other industrial applications. Further investigation is needed to fully understand the properties and potential uses of this compound.

InChI:InChI=1/C8H15NO2.ClH/c10-8(11)6-9-7-4-2-1-3-5-7;/h7,9H,1-6H2,(H,10,11);1H

Downstream Products

• 14328-64-4 (R)-methyl 2-amino-2-cyclohexylacetate hydrochloride 

Relevant articles and documents

Recyclable Ligands for the Non-Enzymatic Dynamic Kinetic Resolution of Challenging α-Amino Acids

Structurally simple and inexpensive chiral tridentate ligands were employed for substantially advancing the purely chemical dynamic kinetic resolution (DKR) of unprotected racemic tailor-made α-amino acids (TM-α-AAs), enabling the first DKR of TM-α-AAs bearing tertiary alkyl chains as well as multiple unprotected functional groups. Owing to the operationally convenient conditions, virtually complete stereoselectivity, and full recyclability of the source of chirality, this method should find wide applications for the preparation of TM-α-AAs, especially on large scale. The non-enzymatic dynamic kinetic resolution of racemic α-amino acids bearing tertiary alkyl chains and multiple unprotected functional groups is based on the enantioselective formation of nickel(II) complexes and their hydrolysis under convenient conditions. The specially designed chiral ligands are inexpensive and can be quantitatively recycled.