Cas 1192887-54-9,(R)-ethyl 5-formyl-5-benzyl-4,5-dihydro-1H-pyrazole-3-carboxylate

1192887-54-9

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Basic information

Product Name: (R)-ethyl 5-formyl-5-benzyl-4,5-dihydro-1H-pyrazole-3-carboxylate
Synonyms: (R)-ethyl 5-formyl-5-benzyl-4,5-dihydro-1H-pyrazole-3-carboxylate
CAS NO:1192887-54-9
Molecular Formula:
Molecular Weight: 260.293
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: (R)-ethyl 5-formyl-5-benzyl-4,5-dihydro-1H-pyrazole-3-carboxylate(CAS DataBase Reference)
NIST Chemistry Reference: (R)-ethyl 5-formyl-5-benzyl-4,5-dihydro-1H-pyrazole-3-carboxylate(1192887-54-9)
EPA Substance Registry System: (R)-ethyl 5-formyl-5-benzyl-4,5-dihydro-1H-pyrazole-3-carboxylate(1192887-54-9)

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: 1192887-54-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1192887-54-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,9,2,8,8 and 7 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1192887-54:
(9*1)+(8*1)+(7*9)+(6*2)+(5*8)+(4*8)+(3*7)+(2*5)+(1*4)=199
199 % 10 = 9
So 1192887-54-9 is a valid CAS Registry Number.

1192887-54-9Upstream product

30457-89-7 2-benzylallyl alcohol

1192887-54-9Downstream Products

1192887-54-9Relevant academic research and scientific papers

Catalytic enantioselective 1,3-dipolar cycloadditions of alkyl diazoacetates with α,β-disubstituted acroleins

Gao, Lizhu,Hwang, Geum-Sook,Lee, Mi Young,Ryu, Do Hyun

supporting information; experimental part, p. 5460 - 5462 (2009/12/08)

A catalytic route to highly functionalized chiral 2-pyrazolines by an asymmetric 1,3-dipolar cycloaddition reaction of ethyl diazoacetate with α-substituted and α,β-disubstituted acroleins has been developed; in the presence of chiral (S)-oxazaborolidiniu

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