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3-methyl-4-phenyl-1,2,5-oxadiazole is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

10349-09-4

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10349-09-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 10349-09-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,0,3,4 and 9 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 10349-09:
(7*1)+(6*0)+(5*3)+(4*4)+(3*9)+(2*0)+(1*9)=74
74 % 10 = 4
So 10349-09-4 is a valid CAS Registry Number.

10349-09-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-methyl-4-phenyl-1,2,5-oxadiazole

1.2 Other means of identification

Product number -
Other names Methyl-phenyl-furazan

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:10349-09-4 SDS

10349-09-4Relevant academic research and scientific papers

Synthesis of furoxan derivatives: DABCO-mediated cascade sulfonylation/cyclization reaction of α-nitro-ketoximes

Zhao, Jian-Qiang,Zhou, Ming-Qiang,Zuo, Jian,Xu, Xiao-Ying,Zhang, Xiao-Mei,Yuan, Wei-Cheng

, p. 1560 - 1565 (2015/03/04)

A convenient and efficient method for the synthesis of furoxan derivatives from α-nitro-ketoximes and sulfonyl chlorides is reported. A wide variety of furoxan derivatives were smoothly obtained in good yields via a DABCO-mediated cascade sulfonylation/cy

ORIENTATION IN THE NITRATION OF 3-PHENYL-4-SUBSTITUTED FURAZANS

Zelenov, M. P.,Frolova, G. M.,Mel'nikova, S. F.,Tselinskii, I. V.

, p. 21 - 23 (2007/10/02)

The nitration of 3-phenyl-4-substituted furazans with various nitrating agents was investigated.It is shown that the orientation of the nitro group that is incorporated in the phenyl ring is determined by the substituent in the 4 position of the furazan r

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