Cas 1263575-72-9,(R)-diethyl 1-(3-oxo-2-phenyl-3,3a,4,5,6,7-hexahydro-2H-indazol-3a-yl)hydrazine-1,2-dicarboxylate

1263575-72-9

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Basic information

Product Name: (R)-diethyl 1-(3-oxo-2-phenyl-3,3a,4,5,6,7-hexahydro-2H-indazol-3a-yl)hydrazine-1,2-dicarboxylate
Synonyms: (R)-diethyl 1-(3-oxo-2-phenyl-3,3a,4,5,6,7-hexahydro-2H-indazol-3a-yl)hydrazine-1,2-dicarboxylate
CAS NO:1263575-72-9
Molecular Formula:
Molecular Weight: 388.423
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)-diethyl 1-(3-oxo-2-phenyl-3,3a,4,5,6,7-hexahydro-2H-indazol-3a-yl)hydrazine-1,2-dicarboxylate(CAS DataBase Reference)
NIST Chemistry Reference: (R)-diethyl 1-(3-oxo-2-phenyl-3,3a,4,5,6,7-hexahydro-2H-indazol-3a-yl)hydrazine-1,2-dicarboxylate(1263575-72-9)
EPA Substance Registry System: (R)-diethyl 1-(3-oxo-2-phenyl-3,3a,4,5,6,7-hexahydro-2H-indazol-3a-yl)hydrazine-1,2-dicarboxylate(1263575-72-9)

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: 1263575-72-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1263575-72-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,6,3,5,7 and 5 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1263575-72:
(9*1)+(8*2)+(7*6)+(6*3)+(5*5)+(4*7)+(3*5)+(2*7)+(1*2)=169
169 % 10 = 9
So 1263575-72-9 is a valid CAS Registry Number.

1263575-72-9Upstream product

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1263575-72-9Relevant academic research and scientific papers

Asymmetric α-amination of 4-substituted pyrazolones catalyzed by a chiral Gd(OTf)3/ N,N′-dioxide complex: Highly enantioselective synthesis of 4-amino-5-pyrazolone derivatives

Yang, Zhigang,Wang, Zhen,Bai, Sha,Liu, Xiaohua,Lin, Lili,Feng, Xiaoming

supporting information; experimental part, p. 596 - 599 (2011/04/15)

The asymmetric α-amination of 4-substituted pyrazolones with azodicarboxylates was investigated for the first time, employing an N,N′-dioxide gadolinium(III) complex as the catalyst. The novel transformations exhibited high yield, and 4-amino-5-pyrazolone

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