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CAS

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92197-46-1

(1-Benzylpyrrolidine-2,5-diyl)diMethanol, also known as BDMP, is a versatile chemical compound widely used in the pharmaceutical industry for the synthesis of various drugs and medications. It features a diol molecule with a pyrrolidine ring and a benzyl group, along with two hydroxyl groups attached to the carbon atoms. Known for its reactivity and utility as a building block in the synthesis of complex organic compounds, BDMP also serves as a chiral auxiliary in asymmetric synthesis, contributing to its significance in organic chemistry. Furthermore, its applications extend to the production of flavors and fragrances, highlighting its value in the chemical industry.

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  • 92197-46-1 Structure

  • Basic information

    1. Product Name: (1-Benzylpyrrolidine-2,5-diyl)diMethanol
    2. Synonyms: (1-Benzylpyrrolidine-2,5-diyl)diMethanol;(1-Benzyl-5-hydroxymethyl-pyrrolidin-2-yl)-methanol
    3. CAS NO:92197-46-1
    4. Molecular Formula: C13H19NO2
    5. Molecular Weight: 221.29546
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 92197-46-1.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: (1-Benzylpyrrolidine-2,5-diyl)diMethanol(CAS DataBase Reference)
    10. NIST Chemistry Reference: (1-Benzylpyrrolidine-2,5-diyl)diMethanol(92197-46-1)
    11. EPA Substance Registry System: (1-Benzylpyrrolidine-2,5-diyl)diMethanol(92197-46-1)

  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 92197-46-1(Hazardous Substances Data)

92197-46-1 Usage

Uses

Used in Pharmaceutical Industry:
BDMP is utilized as a key intermediate in the synthesis of various drugs and medications, leveraging its versatile reactivity and structural features to facilitate the creation of complex organic compounds.
Used in Organic Chemistry:
In the realm of organic chemistry, BDMP serves as a chiral auxiliary for asymmetric synthesis, playing a crucial role in the development of enantioselective reactions and the production of chiral molecules with specific spatial arrangements.
Used in Flavor and Fragrance Industry:
BDMP is employed in the production of certain flavors and fragrances, capitalizing on its chemical properties to contribute to the creation of unique and desirable scents and tastes in various consumer products.

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

-

, (2008/06/13)

The present invention provides diazabicyclooctane derivatives of formula (I): and pharmaceutically acceptable salts thereof, wherein the group represents R1 and R2 are selected independently from H, (C1-C6)alkyl

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,

3-Alkenyl-1-azabicyclo(3.2.0)hept-2-ene-2-carboxylic acid compounds

-

, (2008/06/13)

The invention relates to an antimicrobial compound of the formula: STR1 in which R1 is carboxy or protected carboxy, R2 is hydroxy(lower)alkyl or protected hydroxy(lower)alkyl, R3 and R4 are each hydrogen or low

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