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1-Triazene, 1,3-bis(4-iodophenyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

62807-94-7

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62807-94-7 Usage

Classification

Organic compound, Triazene

Function

Potent and selective inhibitor of mutant BRAFV600E, a common oncogenic driver in human cancer cells

Potential use

Cancer therapy, particularly for melanoma and other solid tumors

Status

Has shown promising results in preclinical studies as a targeted therapy for cancer, but requires further research and clinical trials to fully understand its safety and efficacy.

Check Digit Verification of cas no

The CAS Registry Mumber 62807-94-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,2,8,0 and 7 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 62807-94:
(7*6)+(6*2)+(5*8)+(4*0)+(3*7)+(2*9)+(1*4)=137
137 % 10 = 7
So 62807-94-7 is a valid CAS Registry Number.

62807-94-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-iodo-N-[(4-iodophenyl)diazenyl]aniline

1.2 Other means of identification

Product number -
Other names 1,3-Bis-(4-jod-phenyl)-triazen

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:62807-94-7 SDS

62807-94-7Downstream Products

62807-94-7Relevant academic research and scientific papers

Nitrosation with Sodium Hexanitrocobaltate(III)

Stefane, Bogdan,Kocevar, Marijan,Polanc, Slovenko

, p. 7165 - 7169 (2007/10/03)

Na3Co(NO2)6 has been investigated as a new reagent for the nitrosation of various substrates containing an amino functionality. Reactions took place in an aqueous solution of the reagent. The pH of the reaction mixture remained in the range 4.3-5. Thus, hydrazides were transformed to the corresponding acyl azides, and the reactions with arenesulfonyl hydrazines afforded arenesulfonyl azides. Treatment of aromatic amines with Na3Co(NO2)6 gave 1,3-diaryltriazenes in excellent yields; coupling of the initially formed diazo compound to the electron rich aromatic ring was also observed. Nitrosation of aliphatic amines was not possible due to complex formation with the reagent.

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