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1198-98-7

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1198-98-7 Usage

Synthesis Reference(s)

Journal of Heterocyclic Chemistry, 26, p. 125, 1989 DOI: 10.1002/jhet.5570260122The Journal of Organic Chemistry, 50, p. 1182, 1985 DOI: 10.1021/jo00208a008

Check Digit Verification of cas no

The CAS Registry Mumber 1198-98-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,1,9 and 8 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1198-98:
(6*1)+(5*1)+(4*9)+(3*8)+(2*9)+(1*8)=97
97 % 10 = 7
So 1198-98-7 is a valid CAS Registry Number.
InChI:InChI=1/C9H8N2O/c1-7-10-9(11-12-7)8-5-3-2-4-6-8/h2-6H,1H3

1198-98-7 Well-known Company Product Price

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  • Alfa Aesar

  • (B20145)  5-Methyl-3-phenyl-1,2,4-oxadiazole, 97%   

  • 1198-98-7

  • 1g

  • 546.0CNY

  • Detail
  • Alfa Aesar

  • (B20145)  5-Methyl-3-phenyl-1,2,4-oxadiazole, 97%   

  • 1198-98-7

  • 5g

  • 2185.0CNY

  • Detail

1198-98-7SDS

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 5-METHYL-3-PHENYL-1,2,4-OXADIAZOLE

1.2 Other means of identification

Product number -
Other names 3-phenyl-5-methyl-1,2,4-oxadiazole

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:1198-98-7 SDS

1198-98-7Relevant articles and documents

The reaction of amidoximes with carboxylic acids or their esters under high-pressure conditions

Baikov,Stashina,Chernoburova,Krylov,Zavarzin,Kofanov

, p. 347 - 350 (2019)

3,5-Disubstituted 1,2,4-oxadiazoles were synthesized by the reaction of amidoximes with carboxylic acids or their esters under high-pressure conditions (10 kbar). The reaction proceeds without the use of other reagents or catalysts. Both aliphatic and aro

Reaction of amidoximes with acetonitrile at high pressure

Baykov, Sergey V.,Zharov, Aleksey A.,Stashina, Galina A.,Zavarzin, Igor V.,Kofanov, Evgeniy R.

, p. 264 - 265 (2016)

Reaction of amidoximes with acetonitrile giving 1,2,4-oxadiazoles occurs at 80-100 °C under a pressure of 10 Kbar without catalysts.

Imidazole hydrochloride promoted synthesis of 3,5-disubstituted-1,2,4-oxadiazoles

Wang, Xuetong,Wang, Yin,Liu, Xiaoling,He, Tingshu,Li, Lingli,Wu, Huili,Zhou, Shangjun,Li, Dan,Liao, Siwei,Xu, Ping,Huang, Xing,Yuan, Jianyong

supporting information, (2021/10/14)

Imidazole hydrochloride as an additive promotes the reaction of amidoximes and DMA derivatives to generated 3,5-disubstituted-1,2,4-oxadiazoles in low to excellent yields without the use of coupling reagents, oxidants, strong acids or bases and other additives.

Efficient insecticidal aerosol and preparation method thereof

-

Paragraph 0035; 0046-0048; 0053-0054; 0081; 0092-0094; 0099, (2020/10/30)

The invention provides an efficient insecticidal aerosol, which comprises the following components in percentage by weight: 0.1-0.5wt% of a component A, i.e. a 1, 2, 4-diazole derivative shown as a formula I, 1-1.5wt% of a component B, i.e. a marigold ext

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