Cas 925703-87-3,3-Oxazolidinecarboxylic acid, 4-[(R)-hydroxy(2-hydroxy-4,5-dimethoxyphenyl)methyl]-2,2-dimethyl-, 1,1-dimethylethyl ester, (4R)-

925703-87-3

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Basic information

Product Name: 3-Oxazolidinecarboxylic acid, 4-[(R)-hydroxy(2-hydroxy-4,5-dimethoxyphenyl)methyl]-2,2-dimethyl-, 1,1-dimethylethyl ester, (4R)-
Synonyms:
CAS NO:925703-87-3
Molecular Formula: C19H29NO7
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: 3-Oxazolidinecarboxylic acid, 4-[(R)-hydroxy(2-hydroxy-4,5-dimethoxyphenyl)methyl]-2,2-dimethyl-, 1,1-dimethylethyl ester, (4R)-(CAS DataBase Reference)
NIST Chemistry Reference: 3-Oxazolidinecarboxylic acid, 4-[(R)-hydroxy(2-hydroxy-4,5-dimethoxyphenyl)methyl]-2,2-dimethyl-, 1,1-dimethylethyl ester, (4R)-(925703-87-3)
EPA Substance Registry System: 3-Oxazolidinecarboxylic acid, 4-[(R)-hydroxy(2-hydroxy-4,5-dimethoxyphenyl)methyl]-2,2-dimethyl-, 1,1-dimethylethyl ester, (4R)-(925703-87-3)

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: 925703-87-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 925703-87-3 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 3 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 925703-87:
(8*9)+(7*2)+(6*5)+(5*7)+(4*0)+(3*3)+(2*8)+(1*7)=183
183 % 10 = 3
So 925703-87-3 is a valid CAS Registry Number.

925703-87-3Upstream product

925703-87-3Downstream Products

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

925703-87-3Relevant 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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