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155935-60-7

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155935-60-7 Usage

General Description

2,4-Pyrrolidinedimethanol,3-amino, (2R,3R,4R)-(9CI) is a compound with the molecular formula C7H15NO2. This chemical features a pyrrolidine ring with two hydroxyl groups and an amino group attached to the third carbon. It has a chiral center and exists as a pair of enantiomers, with the (2R,3R,4R) configuration being one of the possible stereoisomers. 2,4-Pyrrolidinedimethanol,3-amino-,(2R,3R,4R)-(9CI) has potential applications in the pharmaceutical and chemical industries due to its chiral nature, which makes it useful for asymmetric synthesis and as a chiral resolving agent. It can also be used as a building block for the synthesis of various organic compounds.

Check Digit Verification of cas no

The CAS Registry Mumber 155935-60-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,5,9,3 and 5 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 155935-60:
(8*1)+(7*5)+(6*5)+(5*9)+(4*3)+(3*5)+(2*6)+(1*0)=157
157 % 10 = 7
So 155935-60-7 is a valid CAS Registry Number.

155935-60-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name ((2R,3R,4R)-3-Amino-4-hydroxymethyl-pyrrolidin-2-yl)-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:155935-60-7 SDS

155935-60-7Downstream Products

155935-60-7Relevant articles and documents

IOOC route to substituted chiral pyrrolidines. Potential glycosidase inhibitors

Falb, Eliezer,Bechor, Yosi,Nudelman, Abraham,Hassner, Alfred,Albeck, Amnon,Gottlieb, Hugo E.

, p. 498 - 506 (2007/10/03)

Branched-chain five-membered ring aza-sugar analogues, synthesized from amino acids by an intramolecular oxime-olefin cycloaddition reaction, the IOOC route, were found to be selective glycosidase inhibitors. The derivative 2,4(S)-di(hydroxymethyl)-3(S)-aminopyrrolidine, obtained from D-serine, was about 1 order of potency more active than its enantiomer obtained from L- serine.

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