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117957-62-7

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117957-62-7 Usage

General Description

(1R,3S)-(3-Aminocyclopentyl) methanol is a chemical compound with a cyclopentane ring containing an amine and a hydroxyl group. It is a chiral molecule, meaning it exists in two mirror image forms. (1R,3S)-(3-Aminocyclopentyl) methanol is primarily used in the synthesis of pharmaceuticals and agrochemicals. The presence of the amine and hydroxyl groups makes it a versatile building block for the production of various chemical compounds. Its unique structural features make it a valuable intermediate in organic synthesis and it has potential applications in the pharmaceutical industry for the development of new drugs. Additionally, it can be utilized in the preparation of various complex organic molecules and can serve as a precursor in the production of other important compounds.

Check Digit Verification of cas no

The CAS Registry Mumber 117957-62-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,7,9,5 and 7 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 117957-62:
(8*1)+(7*1)+(6*7)+(5*9)+(4*5)+(3*7)+(2*6)+(1*2)=157
157 % 10 = 7
So 117957-62-7 is a valid CAS Registry Number.

117957-62-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name (1R,3S)-(3-Aminocyclopentyl) methanol

1.2 Other means of identification

Product number -
Other names -

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:117957-62-7 SDS

117957-62-7Relevant articles and documents

Synthesis and evaluation of cyclopentane-based muraymycin analogs targeting MraY

Kwak, Seung-Hwa,Lim, Won Young,Hao, Aili,Mashalidis, Ellene H.,Kwon, Do-Yeon,Jeong, Pyeonghwa,Kim, Mi Jung,Lee, Seok-Yong,Hong, Jiyong

, (2021/02/21)

Antibiotic resistance is one of the most challenging global health issues and presents an urgent need for the development of new antibiotics. In this regard, phospho-MurNAc-pentapeptide translocase (MraY), an essential enzyme in the early stages of peptid

An efficient procedure for the preparation of (1S,3R)- and (1S,3S)-1-amino-3-(hydroxymethyl)cyclopentanes

Rapoport, Henry,Chen, Yuewu,Mohareb, Rafat M.,Ahn, Jin Hee,Sim, Tae Bo,Ho, Jonathan Z.

, p. 1153 - 1156 (2007/10/03)

Enantiomerically pure (1S,3S)- and (1S,3R)-1-amino-3-(hydroxymethyl) cyclopentanes have been efficiently synthesized from L-aspartic acid. The title compounds are isosteres of ribose and may be used to construct nucleoside analogs with important antiviral

Synthesis of cyclopentane analogs of 1-(2',3'-dideoxy-β-glycero-pentofuranosyl)pyrimidine nucleosides

Hronowski,Szarek

, p. 61 - 70 (2007/10/02)

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