Cas 1394836-89-5,1-(3,5-dimethylbenzoyl)-5,7-dimethylbenzo[c]isoxazol-3(1H)-one

1394836-89-5

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Basic information

Product Name: 1-(3,5-dimethylbenzoyl)-5,7-dimethylbenzo[c]isoxazol-3(1H)-one
Synonyms: 1-(3,5-dimethylbenzoyl)-5,7-dimethylbenzo[c]isoxazol-3(1H)-one
CAS NO:1394836-89-5
Molecular Formula:
Molecular Weight: 295.338
EINECS: N/A
Product Categories: N/A
Mol File: 1394836-89-5.mol
Article Data: 1

Chemical Properties

Melting Point: N/A
Boiling Point: N/A
Flash Point: N/A
Appearance: N/A
Density: N/A
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: 1-(3,5-dimethylbenzoyl)-5,7-dimethylbenzo[c]isoxazol-3(1H)-one(CAS DataBase Reference)
NIST Chemistry Reference: 1-(3,5-dimethylbenzoyl)-5,7-dimethylbenzo[c]isoxazol-3(1H)-one(1394836-89-5)
EPA Substance Registry System: 1-(3,5-dimethylbenzoyl)-5,7-dimethylbenzo[c]isoxazol-3(1H)-one(1394836-89-5)

Safety Data

Hazard Codes: N/A
Statements: N/A
Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 1394836-89-5(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1394836-89-5 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,9,4,8,3 and 6 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1394836-89:
(9*1)+(8*3)+(7*9)+(6*4)+(5*8)+(4*3)+(3*6)+(2*8)+(1*9)=215
215 % 10 = 5
So 1394836-89-5 is a valid CAS Registry Number.

1394836-89-5Upstream product

62034-72-4 N-hydroxy-3,5-dimethylbenzamide

1394836-89-5Downstream Products

1394836-89-5Relevant articles and documents

Pd(II)-catalyzed synthesis of benzisoxazolones from benzohydroxamic acids via C-H activation

Gao, Xi-Ai,Yan, Ru-Long,Wang, Xian-Xue,Yan, Hao,Li, Jian,Guo, Han,Huang, Guo-Sheng

, p. 7700 - 7705 (2012/10/29)

A Pd-catalyzed method for the synthesis of benzisoxazolones from benzohydroxamic acids using Oxone as an oxidant in a one-pot procedure has been developed. In this process, the reaction appears to be suitable for construction of various benzisoxazolones.

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