Cas 925704-01-4,tert-butyl (1R,2R)-1-(2-allyloxy-4,5-dimethoxyphenyl)-1,3-dihydroxypropan-2-ylcarbamate

925704-01-4

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Basic information

Product Name: tert-butyl (1R,2R)-1-(2-allyloxy-4,5-dimethoxyphenyl)-1,3-dihydroxypropan-2-ylcarbamate
Synonyms: tert-butyl (1R,2R)-1-(2-allyloxy-4,5-dimethoxyphenyl)-1,3-dihydroxypropan-2-ylcarbamate
CAS NO:925704-01-4
Molecular Formula:
Molecular Weight: 383.442
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: tert-butyl (1R,2R)-1-(2-allyloxy-4,5-dimethoxyphenyl)-1,3-dihydroxypropan-2-ylcarbamate(CAS DataBase Reference)
NIST Chemistry Reference: tert-butyl (1R,2R)-1-(2-allyloxy-4,5-dimethoxyphenyl)-1,3-dihydroxypropan-2-ylcarbamate(925704-01-4)
EPA Substance Registry System: tert-butyl (1R,2R)-1-(2-allyloxy-4,5-dimethoxyphenyl)-1,3-dihydroxypropan-2-ylcarbamate(925704-01-4)

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: 925704-01-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 925704-01-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,2,5,7,0 and 4 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 925704-01:
(8*9)+(7*2)+(6*5)+(5*7)+(4*0)+(3*4)+(2*0)+(1*1)=164
164 % 10 = 4
So 925704-01-4 is a valid CAS Registry Number.

925704-01-4Upstream product

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925704-01-4Relevant academic research and scientific papers

Synthesis of protected chiral vicinal diaminoalcohols by diastereoselective intramolecular benzylic substitution from bistrichloroacetimidates

Rondot, Christophe,Retailleau, Pascal,Zhu, Jieping

, p. 247 - 250 (2007/10/03)

(Chemical Equation Presented) An efficient synthesis of chiral dihydrooxazines (2) from 1-aryl-2-amino-propane-1,3-diols (1) via the corresponding bistrichloroacetimidate intermediates has been developed. In this transformation, one trichloroacetimidate a

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