Cas 1268833-22-2,(R)-naphthalen-2-yl 2-((4-methoxyphenylsulfonamido)(p-tolyl)methyl)acrylate

1268833-22-2

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Basic information

Product Name: (R)-naphthalen-2-yl 2-((4-methoxyphenylsulfonamido)(p-tolyl)methyl)acrylate
Synonyms: (R)-naphthalen-2-yl 2-((4-methoxyphenylsulfonamido)(p-tolyl)methyl)acrylate
CAS NO:1268833-22-2
Molecular Formula:
Molecular Weight: 487.576
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)-naphthalen-2-yl 2-((4-methoxyphenylsulfonamido)(p-tolyl)methyl)acrylate(CAS DataBase Reference)
NIST Chemistry Reference: (R)-naphthalen-2-yl 2-((4-methoxyphenylsulfonamido)(p-tolyl)methyl)acrylate(1268833-22-2)
EPA Substance Registry System: (R)-naphthalen-2-yl 2-((4-methoxyphenylsulfonamido)(p-tolyl)methyl)acrylate(1268833-22-2)

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: 1268833-22-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1268833-22-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,6,8,8,3 and 3 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1268833-22:
(9*1)+(8*2)+(7*6)+(6*8)+(5*8)+(4*3)+(3*3)+(2*2)+(1*2)=182
182 % 10 = 2
So 1268833-22-2 is a valid CAS Registry Number.

1268833-22-2Upstream product

1268833-22-2Downstream Products

1268833-22-2Relevant academic research and scientific papers

L-Threonine-derived novel bifunctional phosphine-sulfonamide catalyst-promoted enantioselective aza-morita-Baylis-Hillman reaction

Zhong, Fangrui,Wang, Youqing,Han, Xiaoyu,Huang, Kuo-Wei,Lu, Yixin

scheme or table, p. 1310 - 1313 (2011/04/26)

A series of novel bifunctional phosphine-sulfonamide organic catalysts were designed and readily prepared from natural amino acids, and they were utilized to promote enantioselective aza-Morita-Baylis-Hillman (MBH) reactions. l-Threonine-derived phosphine

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