Cas 1294515-31-3,2-((R)-((S)-4-acetyl-3-phenyl-4,5-dihydroisoxazol-4-yl)(p-tolyl)methyl)isoindoline-1,3-dione

1294515-31-3

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Basic information

Product Name: 2-((R)-((S)-4-acetyl-3-phenyl-4,5-dihydroisoxazol-4-yl)(p-tolyl)methyl)isoindoline-1,3-dione
Synonyms:
CAS NO:1294515-31-3
Molecular Formula:
Molecular Weight: 438.483
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: 2-((R)-((S)-4-acetyl-3-phenyl-4,5-dihydroisoxazol-4-yl)(p-tolyl)methyl)isoindoline-1,3-dione(CAS DataBase Reference)
NIST Chemistry Reference: 2-((R)-((S)-4-acetyl-3-phenyl-4,5-dihydroisoxazol-4-yl)(p-tolyl)methyl)isoindoline-1,3-dione(1294515-31-3)
EPA Substance Registry System: 2-((R)-((S)-4-acetyl-3-phenyl-4,5-dihydroisoxazol-4-yl)(p-tolyl)methyl)isoindoline-1,3-dione(1294515-31-3)

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: 1294515-31-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1294515-31-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,9,4,5,1 and 5 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1294515-31:
(9*1)+(8*2)+(7*9)+(6*4)+(5*5)+(4*1)+(3*5)+(2*3)+(1*1)=163
163 % 10 = 3
So 1294515-31-3 is a valid CAS Registry Number.

1294515-31-3Upstream product

698-16-8 benzohydroximoyl chloride

1294515-31-3Downstream Products

1294515-31-3Relevant academic research and scientific papers

Chiral bifunctional thiourea-phosphane organocatalysts in asymmetric allylic amination of Morita-Baylis-Hillman acetates

Deng, Hong-Ping,Wei, Yin,Shi, Min

, p. 1956 - 1960 (2011)

A series of new chiral bifunctional thiourea-phosphane catalysts was synthesized and successfully applied in the catalytic, asymmetric allylic amination of Morita-Baylis-Hillman (MBH) acetates derived from the methyl vinyl ketone (MVK) or ethyl vinyl keto

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