Cas 85364-67-6,3-methyl-4-nitro-5-<2-(2-hydroxy-5-bromophenyl)ethenyl>isoxazole

85364-67-6

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Basic information

Product Name: 3-methyl-4-nitro-5-<2-(2-hydroxy-5-bromophenyl)ethenyl>isoxazole
Synonyms: 3-methyl-4-nitro-5-<2-(2-hydroxy-5-bromophenyl)ethenyl>isoxazole
CAS NO:85364-67-6
Molecular Formula:
Molecular Weight: 325.118
EINECS: N/A
Product Categories: N/A
Mol File: 85364-67-6.mol
Article Data: 2

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: 3-methyl-4-nitro-5-<2-(2-hydroxy-5-bromophenyl)ethenyl>isoxazole(CAS DataBase Reference)
NIST Chemistry Reference: 3-methyl-4-nitro-5-<2-(2-hydroxy-5-bromophenyl)ethenyl>isoxazole(85364-67-6)
EPA Substance Registry System: 3-methyl-4-nitro-5-<2-(2-hydroxy-5-bromophenyl)ethenyl>isoxazole(85364-67-6)

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: 85364-67-6(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 85364-67-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,5,3,6 and 4 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 85364-67:
(7*8)+(6*5)+(5*3)+(4*6)+(3*4)+(2*6)+(1*7)=156
156 % 10 = 6
So 85364-67-6 is a valid CAS Registry Number.

85364-67-6Upstream product

85364-67-6Downstream Products

60410-95-9 (E)-3-(5-bromo-2-hydroxyphenyl)acrylic acid

85364-67-6Relevant articles and documents

Design, synthesis, antimicrobial, anti-inflammatory, and analgesic activity of novel dihydrobenzo furo[3,2-e]isoxazolo[4,5-b]azepin-5(5aH)-ones

Rajanarendar,Govardhan Reddy,Rama Krishna,Shireesha,Reddy,Rajam

, p. 6143 - 6153 (2013)

Novel series of dihydro benzofuro[3,2-e]isoxazolo[4,5-b]azepin-5(5aH)-ones 6 have been synthesized from 3,5-dimethyl-4-nitroisoxazole 1. Compound 1 on treatment with salicyl aldehydes afforded the corresponding nitrostyrylisoxazoles 3, which upon reaction

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