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640292-02-0

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640292-02-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 640292-02-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,4,0,2,9 and 2 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 640292-02:
(8*6)+(7*4)+(6*0)+(5*2)+(4*9)+(3*2)+(2*0)+(1*2)=130
130 % 10 = 0
So 640292-02-0 is a valid CAS Registry Number.
InChI:InChI=1/C11H9NO2/c1-8-2-4-9(5-3-8)11-6-10(7-13)12-14-11/h2-7H,1H3

640292-02-0 Well-known Company Product Price

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  • Aldrich

  • (645044)  5-(4-Methylphenyl)isoxazole-3-carboxaldehyde  97%

  • 640292-02-0

  • 645044-1G

  • 1,529.19CNY

  • Detail
  • Aldrich

  • (645044)  5-(4-Methylphenyl)isoxazole-3-carboxaldehyde  97%

  • 640292-02-0

  • 645044-5G

  • 5,275.53CNY

  • Detail

640292-02-0SDS

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 5-(4-methylphenyl)-1,2-oxazole-3-carbaldehyde

1.2 Other means of identification

Product number -
Other names 5-(p-tolyl)isoxazole-3-carbaldehyde

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:640292-02-0 SDS

640292-02-0Relevant articles and documents

Substituted 1-(isoxazol-3-yl)methyl-1H-1,2,3-triazoles: Synthesis, palladium(II) complexes, and high-turnover catalysis in aqueous media

Bumagin, Nikolay A.,Kletskov, Alexey V.,Petkevich, Sergey K.,Kolesnik, Iryna A.,Lyakhov, Alexander S.,Ivashkevich, Ludmila S.,Baranovsky, Alexander V.,Kurman, Peter V.,Potkin, Vladimir I.

, p. 3578 - 3588 (2018/05/28)

New substituted 3-((1H-1,2,3-triazol-1-yl)methyl)-5-arylisoxazoles (aryl = Ph, p-Tol) and 2-(5-phenylisoxazol-3-yl)-5-(2-(1-((5-(p-tolyl)isoxazol-3-yl)methyl)-1H-1,2,3-triazol-4-yl)ethyl)-1,3,4-oxadiazole were synthesized by means of click-chemistry proce

2-Amino-3-cyano-4-(5-arylisoxazol-3-yl)-4H-chromenes: Synthesis and in vitro cytotoxic activity

Akbarzadeh, Tahmineh,Rafinejad, Ali,Mollaghasem, Javad Malekian,Safavi, Maliheh,Fallah-Tafti, Asal,Pordeli, Mahboobeh,Ardestani, Sussan Kabudanian,Shafiee, Abbas,Foroumadi, Alireza

experimental part, p. 386 - 392 (2012/07/27)

A new series of 4-aryl-4H-chromenes bearing a 5-arylisoxazol-3-yl moiety at the C-4 position were prepared as potential anticancer agents. The in vitro cytotoxic activity of the synthesized compounds was investigated against a panel of tumor cell lines in

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