Cas 262844-05-3,methyl (2R,3S)-2-O-t-butyldimethylsilyl-2,3-dihydroxy-3-(p-chlorophenyl)propionate

262844-05-3

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Basic information

Product Name: methyl (2R,3S)-2-O-t-butyldimethylsilyl-2,3-dihydroxy-3-(p-chlorophenyl)propionate
Synonyms: methyl (2R,3S)-2-O-t-butyldimethylsilyl-2,3-dihydroxy-3-(p-chlorophenyl)propionate
CAS NO:262844-05-3
Molecular Formula:
Molecular Weight: 344.911
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: methyl (2R,3S)-2-O-t-butyldimethylsilyl-2,3-dihydroxy-3-(p-chlorophenyl)propionate(CAS DataBase Reference)
NIST Chemistry Reference: methyl (2R,3S)-2-O-t-butyldimethylsilyl-2,3-dihydroxy-3-(p-chlorophenyl)propionate(262844-05-3)
EPA Substance Registry System: methyl (2R,3S)-2-O-t-butyldimethylsilyl-2,3-dihydroxy-3-(p-chlorophenyl)propionate(262844-05-3)

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: 262844-05-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 262844-05-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,6,2,8,4 and 4 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 262844-05:
(8*2)+(7*6)+(6*2)+(5*8)+(4*4)+(3*4)+(2*0)+(1*5)=143
143 % 10 = 3
So 262844-05-3 is a valid CAS Registry Number.

262844-05-3Upstream product

262844-05-3Downstream Products

206346-40-9 methyl (2R,3S)-2,3-dihydroxy-3-(4'-chlorophenyl)propanoate

262844-05-3Relevant academic research and scientific papers

Aldol reactions with erythrulose derivatives: Stereoselective synthesis of differentially protected syn-α,β-dihydroxy esters

Carda,Murga,Falomir,González,Marco

, p. 677 - 683 (2007/10/03)

Boron enolates of 1-O-silylated erythrulose 3,4-acetonides prepared with Brown's chloro-dicyclohexylborane/tertiary amine system have been shown to react with achiral aldehydes in a highly stereoselective way to yield a 1,2- syn/1,3-syn stereoisomer. Thro

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