Cas 363609-35-2,N-[3-(tert-butyl-dimethyl-silanyloxy)-2,3-diphenyl-propionyl]-4-methyl-N-phenyl-benzenesulfonamide

363609-35-2

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Basic information

Product Name: N-[3-(tert-butyl-dimethyl-silanyloxy)-2,3-diphenyl-propionyl]-4-methyl-N-phenyl-benzenesulfonamide
Synonyms: N-[3-(tert-butyl-dimethyl-silanyloxy)-2,3-diphenyl-propionyl]-4-methyl-N-phenyl-benzenesulfonamide
CAS NO:363609-35-2
Molecular Formula:
Molecular Weight: 585.839
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: N-[3-(tert-butyl-dimethyl-silanyloxy)-2,3-diphenyl-propionyl]-4-methyl-N-phenyl-benzenesulfonamide(CAS DataBase Reference)
NIST Chemistry Reference: N-[3-(tert-butyl-dimethyl-silanyloxy)-2,3-diphenyl-propionyl]-4-methyl-N-phenyl-benzenesulfonamide(363609-35-2)
EPA Substance Registry System: N-[3-(tert-butyl-dimethyl-silanyloxy)-2,3-diphenyl-propionyl]-4-methyl-N-phenyl-benzenesulfonamide(363609-35-2)

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: 363609-35-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 363609-35-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,6,3,6,0 and 9 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 363609-35:
(8*3)+(7*6)+(6*3)+(5*6)+(4*0)+(3*9)+(2*3)+(1*5)=152
152 % 10 = 2
So 363609-35-2 is a valid CAS Registry Number.

363609-35-2Upstream product

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363609-35-2Relevant academic research and scientific papers

Synthesis of optically active aldol derivatives through chirality transfer type 1,2-Wittig rearrangement of α-alkoxycarboxamides

Kitagawa, Osamu,Momose, Shu-Ichi,Yamada, Yoichiro,Shiro, Motoo,Taguchi, Takeo

, p. 4865 - 4868 (2007/10/03)

Treatment of chiral α-benzyloxy- or α-propargyloxycarboxamide with tert-BuLi gave β-hydroxycarboxamides (aldol derivatives) in high optical purity through the formation of α-lithiated ethers and the subsquent 1,2-Wittig rearrangement.

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