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92197-46-1

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92197-46-1 Usage

General Description

(1-Benzylpyrrolidine-2,5-diyl)diMethanol, also known as BDMP, is a chemical compound that is commonly used in the pharmaceutical industry for the synthesis of various drugs and medications. It is a diol molecule that contains a pyrrolidine ring and a benzyl group, and it has two hydroxyl groups attached to the carbon atoms. BDMP is known for its versatile reactivity and is often used as a building block for the synthesis of complex organic compounds. It also has applications in the field of organic chemistry as a chiral auxiliary for asymmetric synthesis. Additionally, BDMP is used in the production of certain flavors and fragrances, making it a valuable compound in the chemical industry.

Check Digit Verification of cas no

The CAS Registry Mumber 92197-46-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,2,1,9 and 7 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 92197-46:
(7*9)+(6*2)+(5*1)+(4*9)+(3*7)+(2*4)+(1*6)=151
151 % 10 = 1
So 92197-46-1 is a valid CAS Registry Number.

92197-46-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name (1-benzyl-5-hydroxymethyl-pyrrolidine-2-yl)-methanol

1.2 Other means of identification

Product number -
Other names 1-BENZYL-2,5-PYRROLIDINEDIMETHANOL

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:92197-46-1 SDS

92197-46-1Relevant articles and documents

An improved and scalable process for 3,8-diazabicyclo[3.2.1]octane analogues

Huang, Long Jiang,Teng, Da Wei

experimental part, p. 523 - 526 (2012/01/30)

An improved and scalable process for substituted 3,8-diazabicyclo[3.2.1] octane was developed. N-Benzyl-2,5-dicarbethoxy-pyrrolidine 2 was reduced to N-benzyl-2,5-dihydroxymethylpyrrolidine 9 and subsequently debenzylated to afford N-Boc-2,5-dihydroxymeth

Diazabicyclooctane derivatives and therapeutic uses thereof

-

Page 18, (2008/06/13)

The present invention provides diazabicyclooctane derivatives of formula (I): and pharmaceutically acceptable salts thereof, wherein the group representsR1 and R2 are selected independently from H, (C1-C6)alkyl,

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