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175476-52-5

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175476-52-5 Usage

Chemical Properties

White solid

Uses

Different sources of media describe the Uses of 175476-52-5 differently. You can refer to the following data:
1. A solid phase organic linker for synthesis of tethering carboxylic acids to support.
2. A solid phase organic linker for synthesis of tethering carboxylic acids to support

Check Digit Verification of cas no

The CAS Registry Mumber 175476-52-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,5,4,7 and 6 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 175476-52:
(8*1)+(7*7)+(6*5)+(5*4)+(4*7)+(3*6)+(2*5)+(1*2)=165
165 % 10 = 5
So 175476-52-5 is a valid CAS Registry Number.
InChI:InChI=1/C4H9NO4S/c5-10(8,9)3-1-2-4(6)7/h1-3H2,(H,6,7)(H2,5,8,9)/p-1

175476-52-5 Well-known Company Product Price

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  • Detail
  • Aldrich

  • (86055)  4-Sulfamoylbutyricacid  technical, ≥90% (T)

  • 175476-52-5

  • 86055-2.5G

  • 5,094.18CNY

  • Detail

175476-52-5SDS

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 3-Carboxypropanesulfonamide

1.2 Other means of identification

Product number -
Other names 4-Sulfamoylbutanoic acid

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:175476-52-5 SDS

175476-52-5Relevant articles and documents

An alkanesulfonamide 'safety-catch' linker for solid-phase synthesis

Backes,Ellman

, p. 2322 - 2330 (2007/10/03)

An alkanesulfonamide 'safety-catch' linker has been developed for tethering carboxylic acids to support. Acylation of the sulfonamide support provides a support-bound N-acylsulfonamide that is stable to both basic and strongly nucleophilic reaction condit

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