Cas 1352147-51-3,(3R,5R,6S)-3-((R)-(3-bromo-4-methoxyphenyl)((tert-butyldimethylsilyl)oxy)methyl)-5,6-diphenylmorpholin-2-one

1352147-51-3

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Basic information

Product Name: (3R,5R,6S)-3-((R)-(3-bromo-4-methoxyphenyl)((tert-butyldimethylsilyl)oxy)methyl)-5,6-diphenylmorpholin-2-one
Synonyms: (3R,5R,6S)-3-((R)-(3-bromo-4-methoxyphenyl)((tert-butyldimethylsilyl)oxy)methyl)-5,6-diphenylmorpholin-2-one
CAS NO:1352147-51-3
Molecular Formula:
Molecular Weight: 582.61
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: (3R,5R,6S)-3-((R)-(3-bromo-4-methoxyphenyl)((tert-butyldimethylsilyl)oxy)methyl)-5,6-diphenylmorpholin-2-one(CAS DataBase Reference)
NIST Chemistry Reference: (3R,5R,6S)-3-((R)-(3-bromo-4-methoxyphenyl)((tert-butyldimethylsilyl)oxy)methyl)-5,6-diphenylmorpholin-2-one(1352147-51-3)
EPA Substance Registry System: (3R,5R,6S)-3-((R)-(3-bromo-4-methoxyphenyl)((tert-butyldimethylsilyl)oxy)methyl)-5,6-diphenylmorpholin-2-one(1352147-51-3)

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: 1352147-51-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1352147-51-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,5,2,1,4 and 7 respectively; the second part has 2 digits, 5 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1352147-51:
(9*1)+(8*3)+(7*5)+(6*2)+(5*1)+(4*4)+(3*7)+(2*5)+(1*1)=133
133 % 10 = 3
So 1352147-51-3 is a valid CAS Registry Number.

1352147-51-3Upstream product

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1352147-51-3Relevant academic research and scientific papers

Synthetic studies toward MPC1001: Preparation of a β-hydroxyl-tyrosine derivative

Schuber Jr., Paul T.,Williams, Robert M.

, p. 380 - 382 (2012)

A procedure for the asymmetric synthesis of a novel β-hydroxy-α- amino acid derivative to be used in the preparation of the natural product MPC1001 and analogs has been developed. The amino acid was efficiently prepared in six steps via a Mukaiyama aldol

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