Cas 1027600-45-8,((2R,3S,4R,5S)-5-Benzyloxymethyl-3,4-dimethyl-3-trimethylsilanyl-tetrahydro-furan-2-yl)-acetic acid methyl ester

1027600-45-8

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Basic information

Product Name: ((2R,3S,4R,5S)-5-Benzyloxymethyl-3,4-dimethyl-3-trimethylsilanyl-tetrahydro-furan-2-yl)-acetic acid methyl ester
Synonyms: ((2R,3S,4R,5S)-5-Benzyloxymethyl-3,4-dimethyl-3-trimethylsilanyl-tetrahydro-furan-2-yl)-acetic acid methyl ester
CAS NO:1027600-45-8
Molecular Formula:
Molecular Weight: 364.557
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: ((2R,3S,4R,5S)-5-Benzyloxymethyl-3,4-dimethyl-3-trimethylsilanyl-tetrahydro-furan-2-yl)-acetic acid methyl ester(CAS DataBase Reference)
NIST Chemistry Reference: ((2R,3S,4R,5S)-5-Benzyloxymethyl-3,4-dimethyl-3-trimethylsilanyl-tetrahydro-furan-2-yl)-acetic acid methyl ester(1027600-45-8)
EPA Substance Registry System: ((2R,3S,4R,5S)-5-Benzyloxymethyl-3,4-dimethyl-3-trimethylsilanyl-tetrahydro-furan-2-yl)-acetic acid methyl ester(1027600-45-8)

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: 1027600-45-8(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1027600-45-8 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,2,7,6,0 and 0 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1027600-45:
(9*1)+(8*0)+(7*2)+(6*7)+(5*6)+(4*0)+(3*0)+(2*4)+(1*5)=108
108 % 10 = 8
So 1027600-45-8 is a valid CAS Registry Number.

1027600-45-8Upstream product

1027600-45-8Downstream Products

146980-53-2 (E)-(5S,6S)-7-Benzyloxy-6-hydroxy-4,5-dimethyl-hept-3-enoic acid methyl ester

1027600-45-8Relevant academic research and scientific papers

Acyclic Diastereoselectivity in the Lewis Acid Promoted Additions of Chiral, β-Methyl-Substituted (E)-Crotylsilanes with Achiral Aldehydes

Panek, James S.,Cirillo, Pier F.

, p. 999 - 1002 (1993)

The diastereoselection in the Lewis acid promoted addition of chiral, β-methyl-substituted (E)-crotylsilanes (S)-1a and (R)-1b with α-(benzyloxy)acetaldehyde (2) is reversed from syn to anti by changing the Lewis acid from BF3*OEt2 (non-chelation-controll

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