Cas 1393751-13-7,(R)-N-allyl-N-(1-(tert-butyldimethylsilyloxy)-3-hydroxypropan-2-yl)-4-methylbenzenesulfonamide

1393751-13-7

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Basic information

Product Name: (R)-N-allyl-N-(1-(tert-butyldimethylsilyloxy)-3-hydroxypropan-2-yl)-4-methylbenzenesulfonamide
Synonyms: (R)-N-allyl-N-(1-(tert-butyldimethylsilyloxy)-3-hydroxypropan-2-yl)-4-methylbenzenesulfonamide
CAS NO:1393751-13-7
Molecular Formula:
Molecular Weight: 399.627
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)-N-allyl-N-(1-(tert-butyldimethylsilyloxy)-3-hydroxypropan-2-yl)-4-methylbenzenesulfonamide(CAS DataBase Reference)
NIST Chemistry Reference: (R)-N-allyl-N-(1-(tert-butyldimethylsilyloxy)-3-hydroxypropan-2-yl)-4-methylbenzenesulfonamide(1393751-13-7)
EPA Substance Registry System: (R)-N-allyl-N-(1-(tert-butyldimethylsilyloxy)-3-hydroxypropan-2-yl)-4-methylbenzenesulfonamide(1393751-13-7)

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: 1393751-13-7(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1393751-13-7 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,9,3,7,5 and 1 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1393751-13:
(9*1)+(8*3)+(7*9)+(6*3)+(5*7)+(4*5)+(3*1)+(2*1)+(1*3)=177
177 % 10 = 7
So 1393751-13-7 is a valid CAS Registry Number.

1393751-13-7Upstream product

1393751-13-7Downstream Products

1393751-23-9 N-(((2S,5R)-5-((tert-butyldimethylsilyloxy)methyl)-4-tosylmorpholin-2-yl)methyl)-4-methylbenzenesulfonamide

1393751-13-7Relevant academic research and scientific papers

Stereoselective synthesis of morpholines via copper-promoted oxyamination of alkenes

Sequeira, Fatima C.,Chemler, Sherry R.

, p. 4482 - 4485 (2012)

A new copper(II) 2-ethylhexanoate-promoted addition of an alcohol and an amine across an alkene (oxyamination) is reported. The alcohol addition is intramolecular, while coupling with the amine occurs intermolecularly. Several 2-aminomethyl morpholines we

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