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34637-22-4

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34637-22-4 Usage

General Description

Benzyl N-(3-hydroxypropyl)carbamate is a chemical compound that consists of a benzyl group attached to a carbamate functional group, which in turn is linked to a 3-hydroxypropyl group. It is commonly used as a reagent in organic synthesis and as a pharmaceutical intermediate. BENZYL N-(3-HYDROXYPROPYL)CARBAMATE has potential applications in the field of medicinal chemistry, particularly as a precursor for the synthesis of potential drug candidates. Additionally, benzyl N-(3-hydroxypropyl)carbamate may also have applications in the development of new materials and polymers due to its unique chemical structure. As with any chemical compound, proper handling and safety precautions should be taken when working with benzyl N-(3-hydroxypropyl)carbamate.

Check Digit Verification of cas no

The CAS Registry Mumber 34637-22-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,4,6,3 and 7 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 34637-22:
(7*3)+(6*4)+(5*6)+(4*3)+(3*7)+(2*2)+(1*2)=114
114 % 10 = 4
So 34637-22-4 is a valid CAS Registry Number.
InChI:InChI=1/C11H15NO3/c13-8-4-7-12-11(14)15-9-10-5-2-1-3-6-10/h1-3,5-6,13H,4,7-9H2,(H,12,14)

34637-22-4 Well-known Company Product Price

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  • Aldrich

  • (478709)  BenzylN-(3-hydroxypropyl)carbamate  97%

  • 34637-22-4

  • 478709-25G

  • 1,283.49CNY

  • Detail

34637-22-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name BENZYL N-(3-HYDROXYPROPYL)CARBAMATE

1.2 Other means of identification

Product number -
Other names 3-(benzyloxycarbonylamino)-1-propanol

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:34637-22-4 SDS

34637-22-4Relevant articles and documents

A synthesis of tiruchanduramine and a reinvestigation of its glycosidase inhibitory activity

Buck, Matthew L.,Evans, Daniel M.,Evans, Victoria A.,Herkt, Dominik,Sharp, Hazel,Hollinshead, Jackie,Mitschang, Fabian,Murphy, Patrick J.,Nash, Robert J.,Wenbourne, Jack

, p. 4545 - 4548 (2017)

Tiruchanduramine 1 was prepared using a convergent strategy with the longest linear sequence being eight steps. Synthetic 1, displayed a broader range of inhibition than reported previously and, in addition to α-glucosidases, 1 also inhibits almond β-gluc

METHOD FOR PRODUCING (2S)-2-[(1H-PYRAZOL-1-YL)METHYL]-1,3-OXAZINANE DERIVATIVE

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Paragraph 0290-0292, (2021/05/21)

Provided is a novel process for producing a (2S)-2-[(1H-pyrazol-1-yl)methyl]-1,3-oxazinane derivative. More specifically, provided is a process for producing a (2S)-2-[(1H-pyrazol-1-yl)methyl]-1,3-oxazinane derivative represented by formula (1): the process comprising reacting 3-aminopropan-1-ol with glyoxylic acid.

LOW CONTAMINANT ANTIMICROBIAL VACCINES

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Paragraph 0081; 0093, (2021/05/21)

Disclosed are antimicrobial vaccines comprising oligosaccharide β-(1→6)-glucosamine groups.

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