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L-Threonine, N-(phenylsulfonyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

93474-55-6

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93474-55-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 93474-55-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,3,4,7 and 4 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 93474-55:
(7*9)+(6*3)+(5*4)+(4*7)+(3*4)+(2*5)+(1*5)=156
156 % 10 = 6
So 93474-55-6 is a valid CAS Registry Number.

93474-55-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name (2S,3R)-3-hydroxy-2-(phenylsulfonamido)butanoic acid

1.2 Other means of identification

Product number -
Other names N-(phenylsulfonyl)-L-threonine

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:93474-55-6 SDS

93474-55-6Relevant academic research and scientific papers

New carboxamides bearing benzenesulphonamides: Synthesis, molecular docking and pharmacological properties

Eze, Florence Uchenna,Okoro, Uchechukwu Chris,Ugwu, David Izuchukwu,Okafor, Sunday N.

, (2019/09/18)

Ten new derivatives of benzenesulphonamide bearing carboxamide functionality were synthesized and investigated for their in vitro antimicrobial, antioxidant and in vivo anti-inflammatory activities. Compound 9d inhibited carrageenan induced rat-paw oedema

Design, synthesis and in vitro biochemical activity of novel amino acid sulfonohydrazide inhibitors of MurC

Frlan, Rok,Kovas, Andreja,Blanot, Didier,Gobec, Stanislav,Pecar, Slavko,Obreza, Ales

scheme or table, p. 295 - 310 (2012/04/23)

Mur ligases are essential enzymes involved in the cytoplasmic steps of peptidoglycan synthesis which remain attractive, yet unexploited targets. In order to develop new antibacterial agents, we have designed a series of new MurC and MurD inhibitors bearin

Synthesis and Reactivity of β-Lactones Derived from L-Threonine and Related Amino Acids

Pansare, Sunil V.,Vederas, John C.

, p. 2311 - 2316 (2007/10/02)

The synthesis and nucleophilic ring opening of optically pure N-protected α-amino-β-alkyl β-lactones was investigated.Treatment of N-BOC-L-threonine (8) and N-BOC-L-allo-threonine (9) under modified Mitsunobu conditions (Ph3P, dimethyl azodicarboxylate, -

α-Amino Acids as Chiral Educts for Asymmetric Products. Chirospecific Syntheses of Methyl L-Sibirosaminide and Its C-3 Epimer from L-Allothreonine

Maurer, Peter J.,Knudsen, Christopher G.,Palkowitz, Alan D.,Papoport, Henry

, p. 325 - 332 (2007/10/02)

Efficient syntheses of methyl L-sibirosaminide and its C-3 epimer are described using L-allothreonine as the chiral educt.Amino acylations of organometallics with the lithium salt of N-(phenylsulfonyl)-L-allothreonine constitute the key carbon-carbon bond

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