Cas 1356395-35-1,N-(tert-butyldiphenylsilyl) (2-bromo-4-methoxyphenyl)ethyl methyl sulfoximine

1356395-35-1

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Basic information

Product Name: N-(tert-butyldiphenylsilyl) (2-bromo-4-methoxyphenyl)ethyl methyl sulfoximine
Synonyms: N-(tert-butyldiphenylsilyl) (2-bromo-4-methoxyphenyl)ethyl methyl sulfoximine
CAS NO:1356395-35-1
Molecular Formula:
Molecular Weight: 530.601
EINECS: N/A
Product Categories: N/A
Mol File: 1356395-35-1.mol
Article Data: 1

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-(tert-butyldiphenylsilyl) (2-bromo-4-methoxyphenyl)ethyl methyl sulfoximine(CAS DataBase Reference)
NIST Chemistry Reference: N-(tert-butyldiphenylsilyl) (2-bromo-4-methoxyphenyl)ethyl methyl sulfoximine(1356395-35-1)
EPA Substance Registry System: N-(tert-butyldiphenylsilyl) (2-bromo-4-methoxyphenyl)ethyl methyl sulfoximine(1356395-35-1)

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: 1356395-35-1(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1356395-35-1 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,5,6,3,9 and 5 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1356395-35:
(9*1)+(8*3)+(7*5)+(6*6)+(5*3)+(4*9)+(3*5)+(2*3)+(1*5)=181
181 % 10 = 1
So 1356395-35-1 is a valid CAS Registry Number.

1356395-35-1Upstream product

1356395-35-1Downstream Products

1356395-36-2 (2-bromo-4-methoxyphenyl)ethyl methyl sulfoximine

1356395-35-1Relevant articles and documents

Asymmetric syntheses of S, S-dialkyl-substituted sulfoximines and related heterocycles

Pandey, Ankur G.,McGrath, Matthew J.,Garciamancheno, Olga,Bolm, Carsten

experimental part, p. 3827 - 3838 (2012/01/11)

Enantiomerically enriched forms of a sulfoximine-based myristic acid analogue are prepared using either an asymmetric desymmetrization with a chiral base, or an enantioselective oxidation procedure as key steps. Additionally, a variety of 2-oxa-2-alkyl 3,

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