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38010-31-0

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38010-31-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 38010-31-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,8,0,1 and 0 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 38010-31:
(7*3)+(6*8)+(5*0)+(4*1)+(3*0)+(2*3)+(1*1)=80
80 % 10 = 0
So 38010-31-0 is a valid CAS Registry Number.

38010-31-0SDS

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 2-(benzenesulfonyl)-N-phenylacetamide

1.2 Other means of identification

Product number -
Other names Phenylsulfonessigsaeure-anilid

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:38010-31-0 SDS

38010-31-0Relevant articles and documents

One-pot copper-catalyzed three-component reaction: A modular approach to functionalized 2-quinolones

Kim, Ah Reum,Lim, Hee Nam

, p. 7855 - 7866 (2020/03/11)

A copper-catalyzed three-component annulation for the synthesis of functionalized 2-quinolones was developed. Three reactions including an SN2, a Knoevenagel, and finally C-N bond formation are involved in the designed cascade reaction using 2-bromoacylarenes, 2-iodoacetamide, and nucleophiles as the three components. A new catalytic system was discovered during the study and this modular approach is highly efficient to access functionalized 2-quinolone derivatives, compatible with a broad range of functional groups, scalable, and step-economic. Further derivatization of the obtained product demonstrates the synthetic utility of this method.

α-Phenylsulfonyl-N-arylacetamides (α-phenylsulfonylacetanilides): 1H, 13C and 15N NMR spectral characterization

Kolehmainen, Erkki,Janota, Henryk,Gawinecki, Ryszard,Laihia, Katri,Kauppinen, Reijo

, p. 384 - 385 (2007/10/03)

1H and 13C NMR chemical shift assignments for 11 α-phenylsulfonylacetanilides and 15N NMR chemical shifts for four representative congeners are reported. The 1H and 13C chemical shift assignments are based on DQF COSY and PFG 1H, 13C HMQC/HMBC experiments. The 15N NMR chemical shifts were determined by PFG 1H, 15N HMBC experiments. The correlation analyses with Hammett-type substituent constants gave a significant result with δ(C-1) in the aniline ring. Copyright

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