Cas 1326775-72-7,5-(2,4-dimethylphenyl)-7-methyl-5,6-diazaspiro[2.4]hept-6-en-4-one

1326775-72-7

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Basic information

Product Name: 5-(2,4-dimethylphenyl)-7-methyl-5,6-diazaspiro[2.4]hept-6-en-4-one
Synonyms: 5-(2,4-dimethylphenyl)-7-methyl-5,6-diazaspiro[2.4]hept-6-en-4-one
CAS NO:1326775-72-7
Molecular Formula:
Molecular Weight: 228.294
EINECS: N/A
Product Categories: N/A

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: 5-(2,4-dimethylphenyl)-7-methyl-5,6-diazaspiro[2.4]hept-6-en-4-one(CAS DataBase Reference)
NIST Chemistry Reference: 5-(2,4-dimethylphenyl)-7-methyl-5,6-diazaspiro[2.4]hept-6-en-4-one(1326775-72-7)
EPA Substance Registry System: 5-(2,4-dimethylphenyl)-7-methyl-5,6-diazaspiro[2.4]hept-6-en-4-one(1326775-72-7)

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: 1326775-72-7(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1326775-72-7 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,2,6,7,7 and 5 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1326775-72:
(9*1)+(8*3)+(7*2)+(6*6)+(5*7)+(4*7)+(3*5)+(2*7)+(1*2)=177
177 % 10 = 7
So 1326775-72-7 is a valid CAS Registry Number.

1326775-72-7Upstream product

1021876-17-4 N-(2,4-dimethylphenyl)-1-(1-(hydroxyimino)ethyl)cyclopropanecarboxamide

1326775-72-7Downstream Products

1326775-72-7Relevant academic research and scientific papers

Divergent synthesis of fully substituted isoxazoles and spiro-fused pyrazolin-5-ones from cyclopropyl oximes

Fu, Xiaolan,Huang, Peng,Zhou, Guangyuan,Hu, Yinqiao,Dong, Dewen

experimental part, p. 6347 - 6351 (2011/09/12)

Efficient and divergent synthesis of fully substituted isoxazoles and spiro-fused pyrazolin-5-ones is developed from cyclopropyl oximes based on selection of reaction conditions. Under Appel conditions (PPh 3/CBr4), substituted isoxa

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