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62806-39-7

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62806-39-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 62806-39-7 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 6 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 62806-39:
(7*6)+(6*2)+(5*8)+(4*0)+(3*6)+(2*3)+(1*9)=127
127 % 10 = 7
So 62806-39-7 is a valid CAS Registry Number.

62806-39-7SDS

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 3-[5-(4-nitrophenyl)furan-2-yl]prop-2-enoic acid

1.2 Other means of identification

Product number -
Other names 3-[5-(4-nitrophenyl)-2-furyl]acrylic acid

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:62806-39-7 SDS

62806-39-7Relevant articles and documents

Development of molecular probes for second-site screening and design of protein tyrosine phosphatase inhibitors

Vazquez, Jesus,Tautz, Lutz,Ryan, Jennifer J.,Vuori, Kristiina,Mustelin, Tomas,Pellecchia, Maurizio

, p. 2137 - 2143 (2008/02/01)

We report on the design, synthesis, and evaluation of a series of furanyl-salicyl-nitroxide derivatives as effective chemical probes for second-site screening against phosphotyrosine phosphatases (PTPs) using NMR-based techniques. The compounds have been

Synthesis of 2-arylfuro[3,2-c]pyridines and their derivatives

Krutosikova, Alzbeta,Sleziak, Robert

, p. 1627 - 1636 (2007/10/03)

A series of 2-arylfuro[3,2-c]pyridines was synthesized. 3-(5-Aryl-2-furyl)propenoic acids 1a-1h were converted to the acid azides 2a-2h, which in turn were cyclized to give 2-arylfuro[3,2-c]pyridine-4(5H)-ones 4a-4h by heating in Dowtherm. The pyridones 4a-4f were aromatized with phosphorus oxychloride to the 2-aryl-4-chlorofuro[3,2-c]pyridines 5a-5f, which were reduced with zinc and acetic acid to the title compounds 6a-6f. Reacted with phosphorus(V) sulfide, the pyridones 4a-4f yielded the corresponding thiones 7a-7f.

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