Cas 1268464-35-2,(3S,4R)-3-(4-methoxyphenyl)-5-phenyl-4-(phenylsulfonyl)-3,4-dihydro-2H-pyrroline-1-oxide

1268464-35-2

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Basic information

Product Name: (3S,4R)-3-(4-methoxyphenyl)-5-phenyl-4-(phenylsulfonyl)-3,4-dihydro-2H-pyrroline-1-oxide
Synonyms:
CAS NO:1268464-35-2
Molecular Formula:
Molecular Weight: 407.49
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: (3S,4R)-3-(4-methoxyphenyl)-5-phenyl-4-(phenylsulfonyl)-3,4-dihydro-2H-pyrroline-1-oxide(CAS DataBase Reference)
NIST Chemistry Reference: (3S,4R)-3-(4-methoxyphenyl)-5-phenyl-4-(phenylsulfonyl)-3,4-dihydro-2H-pyrroline-1-oxide(1268464-35-2)
EPA Substance Registry System: (3S,4R)-3-(4-methoxyphenyl)-5-phenyl-4-(phenylsulfonyl)-3,4-dihydro-2H-pyrroline-1-oxide(1268464-35-2)

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: 1268464-35-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1268464-35-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,6,8,4,6 and 4 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1268464-35:
(9*1)+(8*2)+(7*6)+(6*8)+(5*4)+(4*6)+(3*4)+(2*3)+(1*5)=182
182 % 10 = 2
So 1268464-35-2 is a valid CAS Registry Number.

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1268464-35-2Relevant academic research and scientific papers

Synthesis of chiral cyclic nitrones by asymmetric addition of β-ketosulfones to nitroalkenes followed by reductive cyclization

Mancheno, Olga Garci,Tangen, Pia,Rohlmann, Renate,Froehlich, Roland,Aleman, Jose

, p. 984 - 992 (2011)

The first organocatalytic addition of β-ketosulfones to nitroalkenes catalyzed by thiourea cinchona alkaloids is presented. The readily obtained addition products were selectively transformed into chiral nitrones by reduction of the nitro group and in sit

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