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Phenol, 3-[(7-nitro-2,1,3-benzoxadiazol-4-yl)amino]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

101237-24-5

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101237-24-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 101237-24-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,1,2,3 and 7 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 101237-24:
(8*1)+(7*0)+(6*1)+(5*2)+(4*3)+(3*7)+(2*2)+(1*4)=65
65 % 10 = 5
So 101237-24-5 is a valid CAS Registry Number.

101237-24-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name N-(3-Hydroxyphenyl)-4-amino-7-nitrobenz-2,1,3-oxadiazol

1.2 Other means of identification

Product number -
Other names 3-[(7-nitro-2,1,3-benzoxadiazol-4-yl)amino]phenol

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:101237-24-5 SDS

101237-24-5Downstream Products

101237-24-5Relevant academic research and scientific papers

Derivatization of Amines with 4-Substituted 7-Nitrobenzofurazans

Heberer, H.,Kersting, H.,Matschiner, H.

, p. 487 - 504 (2007/10/02)

Electrophilic derivatives of 4-nitro-benzofurazan with different reactivities were used to synthesize 28 new mono- and disubstituted 4-amino-7-nitrobenzofurazans 2b, 2d, 2f-2i, 2l, 2m-2n, 3b-3f, 3h-3j, 4c-4d, 4f-4k, 4m, 4o-4p.A reaction mechanism is proposed on the basis of the differences of the reactivities and a preliminary kinetic examination.The acid character of the N-H-function in monosubstituted compounds is demonstrated by means of spectroscopical investigation of pKa-values.Data from i.r., u.v./vis, and fluorescence studies are offered.

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