Cas 1255534-53-2,(R)-(2-benzyl-5-methyl-3-(naphthalen-2-yl)-2,3-dihydroisoxazol-4-yl)(3,5-dimethyl-1H-pyrazol-1-yl)methanone

1255534-53-2

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Basic information

Product Name: (R)-(2-benzyl-5-methyl-3-(naphthalen-2-yl)-2,3-dihydroisoxazol-4-yl)(3,5-dimethyl-1H-pyrazol-1-yl)methanone
Synonyms: (R)-(2-benzyl-5-methyl-3-(naphthalen-2-yl)-2,3-dihydroisoxazol-4-yl)(3,5-dimethyl-1H-pyrazol-1-yl)methanone
CAS NO:1255534-53-2
Molecular Formula:
Molecular Weight: 423.514
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)-(2-benzyl-5-methyl-3-(naphthalen-2-yl)-2,3-dihydroisoxazol-4-yl)(3,5-dimethyl-1H-pyrazol-1-yl)methanone(CAS DataBase Reference)
NIST Chemistry Reference: (R)-(2-benzyl-5-methyl-3-(naphthalen-2-yl)-2,3-dihydroisoxazol-4-yl)(3,5-dimethyl-1H-pyrazol-1-yl)methanone(1255534-53-2)
EPA Substance Registry System: (R)-(2-benzyl-5-methyl-3-(naphthalen-2-yl)-2,3-dihydroisoxazol-4-yl)(3,5-dimethyl-1H-pyrazol-1-yl)methanone(1255534-53-2)

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: 1255534-53-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1255534-53-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,5,5,5,3 and 4 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1255534-53:
(9*1)+(8*2)+(7*5)+(6*5)+(5*5)+(4*3)+(3*4)+(2*5)+(1*3)=152
152 % 10 = 2
So 1255534-53-2 is a valid CAS Registry Number.

1255534-53-2Upstream product

22661-26-3 (Z)-N-(naphthalen-2-ylmethylene)-1-phenylmethanamine oxide

1255534-53-2Downstream Products

1255534-53-2Relevant academic research and scientific papers

Catalytic enantioselective 1,3-dipolar cycloadditions of nitrones with propioloylpyrazoles and acryloylpyrazoles induced by chiral π-cation catalysts

Sakakura, Akira,Hori, Masahiro,Fushimi, Makoto,Ishihara, Kazuaki

supporting information; experimental part, p. 15550 - 15552 (2011/02/22)

A chiral copper(II) complex of 3-(2-naphthyl)-l-alanine amide successfully catalyzes the enantioselective 1,3-dipolar cycloaddition reaction of nitrones with propioloylpyrazole and acryloylpyrazole derivatives. The asymmetric environment created by intram

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