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1-Boc-2-(4-nitrobenzenesulfonyl)hydrazine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

333440-71-4

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333440-71-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 333440-71-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,3,3,4,4 and 0 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 333440-71:
(8*3)+(7*3)+(6*3)+(5*4)+(4*4)+(3*0)+(2*7)+(1*1)=114
114 % 10 = 4
So 333440-71-4 is a valid CAS Registry Number.

333440-71-4 Well-known Company Product Price

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  • Aldrich

  • (725420)  1-Boc-2-(4-nitrobenzenesulfonyl)hydrazine  97%

  • 333440-71-4

  • 725420-5G

  • 697.32CNY

  • Detail

333440-71-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name tert-butyl N-[(4-nitrophenyl)sulfonylamino]carbamate

1.2 Other means of identification

Product number -
Other names 1-Boc-2-(4-nitrobenzenesulfonyl)hydrazine

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:333440-71-4 SDS

333440-71-4Relevant academic research and scientific papers

Regio- and Stereocontrolled Synthesis of 3-Substituted 1,2-Diazetidines by Asymmetric Allylic Amination of Vinyl Epoxide

Rajkumar, Sundaram,Clarkson, Guy J.,Shipman, Michael

supporting information, p. 2058 - 2061 (2017/04/27)

Pd-catalyzed asymmetric allylic amination of rac-vinyl epoxide with unsymmetrical 1,2-hydrazines proceeds with excellent regio- and stereocontrol, which after further ring closure provides differentially protected 3-vinyl-1,2-diazetidines in good yields.

Synthesis and reactivity of 2,3-dihydro-1H-2,3-benzodiazepine-1,4(5H)-dione

Bihel, Frederic J.-J.,Hellal, Malik,Bourguignon, Jean-Jacques

, p. 3791 - 3796 (2008/09/17)

Based on an orthogonal protective group strategy dealing with N-protected hydrazine, we established for the first time a highly efficient synthetic pathway leading to 2,3-benzodiazepine-1,4-dione. Moreover, the versatile reactivities exhibited by this 2,3

NOVEL QUINOXALINE DERIVATIVES

-

Page/Page column 195-196, (2008/06/13)

A quinoxalinone derivative of the formula (I): or a pharmaceutically acceptable salt or ester thereof, wherein; ???X is NH, S or the like; ???Y is O or the like; ???the partial structure is, for example, the formula: ???B1, B2, ....., Bn-1 and Bn, (in which n is 4 , 5 or 6) are each independently CH, N or the like; ???B'1, B'2, ....., B'n-1 and B'n (in which n is 4, 5 or 6) are each independently hydrogen or the like; and ???R is hydrogen, lower alkyl or the like.

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