Cas 1023641-45-3,N-[2-(tert-butyldimethylsilanyloxy)ethyl]-N-(2-hydroxyethyl)-4-methyl-benzenesulfonamide

1023641-45-3

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Basic information

Product Name: N-[2-(tert-butyldimethylsilanyloxy)ethyl]-N-(2-hydroxyethyl)-4-methyl-benzenesulfonamide
Synonyms: N-[2-(tert-butyldimethylsilanyloxy)ethyl]-N-(2-hydroxyethyl)-4-methyl-benzenesulfonamide
CAS NO:1023641-45-3
Molecular Formula:
Molecular Weight: 373.589
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-[2-(tert-butyldimethylsilanyloxy)ethyl]-N-(2-hydroxyethyl)-4-methyl-benzenesulfonamide(CAS DataBase Reference)
NIST Chemistry Reference: N-[2-(tert-butyldimethylsilanyloxy)ethyl]-N-(2-hydroxyethyl)-4-methyl-benzenesulfonamide(1023641-45-3)
EPA Substance Registry System: N-[2-(tert-butyldimethylsilanyloxy)ethyl]-N-(2-hydroxyethyl)-4-methyl-benzenesulfonamide(1023641-45-3)

Safety Data

Hazard Codes: N/A
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Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 1023641-45-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1023641-45-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,2,3,6,4 and 1 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1023641-45:
(9*1)+(8*0)+(7*2)+(6*3)+(5*6)+(4*4)+(3*1)+(2*4)+(1*5)=103
103 % 10 = 3
So 1023641-45-3 is a valid CAS Registry Number.

1023641-45-3Upstream product

1023641-45-3Downstream Products

1023641-47-5 N-(2-((tert-butyldimethylsilyl)oxy)ethyl)-4-methyl-N-(2–oxoethyl)benzenesulfonamide

1023641-45-3Relevant academic research and scientific papers

The stereochemical course of bromoetherification of enynes

Christopher Braddock,Bhuva, Roshni,Perez-Fuertes, Yolanda,Pouwer, Rebecca,Roberts, Craig A.,Ruggiero, Andrea,Stokes, Elaine S. E.,White, Andrew J. P.

, p. 1419 - 1421 (2008/12/21)

Enynes undergo stereoselective syn intramolecular bromoetherification; the stereochemical course of the reaction was elucidated by X-ray crystallographic studies and by stereospecific synthesis of authentic bromoallenes. The Royal Society of Chemistry.

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