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Benzenesulfonyl isocyanate, 2-nitro- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

68322-82-7

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68322-82-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 68322-82-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,8,3,2 and 2 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 68322-82:
(7*6)+(6*8)+(5*3)+(4*2)+(3*2)+(2*8)+(1*2)=137
137 % 10 = 7
So 68322-82-7 is a valid CAS Registry Number.

68322-82-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-nitro-N-(oxomethylidene)benzenesulfonamide

1.2 Other means of identification

Product number -
Other names Benzenesulfonyl isocyanate,2-nitro

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:68322-82-7 SDS

68322-82-7Relevant academic research and scientific papers

Synthesis of the oxygenated pactamycin core

Knapp, Spencer,Younong, Yu

, p. 1359 - 1362 (2008/04/18)

Figure presented Pactamycin, one of the most complex and densely functionalized aminocyclitol antibiotics known, presents synthetic challenges that include reactivity and sterics, relative and absolute stereochemistry, and functional group compatibility a

Palladium-catalyzed carbonylation of (arylsulfonyliminoido)-benzenes to arylsulfonyl isocyanates

Besenyei,Simandi

, p. 2839 - 2842 (2007/10/02)

In the presence of palladium complexes as catalysts, carbonylation of (arylsulfonyliminoiodo)benzenes to arylsulfonyl isocyanates can be accomplished with 50-80% yield.

Acyl and Sulfonyl Isocyanates ib β-Lactam Synthesis

Barrett, Anthony G. M.,Betts, Michael J.,Fenwick, Ashley

, p. 169 - 175 (2007/10/02)

The preparation of β-lactams from the reactions of several acyl and sulfonyl activated isocyanates with alkenes was studied.Three compounds, (2,2,2-trichloroethoxy)sulfonyl, 2,2,2-trichloroethane sulfonyl, and trifluoroacetyl isocyanates, were shown to be

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