Cas 118893-75-7,Benzoic acid (2R,3R,6S)-4-(tert-butyl-dimethyl-silanyloxy)-2-furan-2-yl-6-methoxy-3,6-dihydro-2H-pyran-3-yl ester

118893-75-7

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Basic information

Product Name: Benzoic acid (2R,3R,6S)-4-(tert-butyl-dimethyl-silanyloxy)-2-furan-2-yl-6-methoxy-3,6-dihydro-2H-pyran-3-yl ester
Synonyms: Benzoic acid (2R,3R,6S)-4-(tert-butyl-dimethyl-silanyloxy)-2-furan-2-yl-6-methoxy-3,6-dihydro-2H-pyran-3-yl ester
CAS NO:118893-75-7
Molecular Formula:
Molecular Weight: 430.573
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: Benzoic acid (2R,3R,6S)-4-(tert-butyl-dimethyl-silanyloxy)-2-furan-2-yl-6-methoxy-3,6-dihydro-2H-pyran-3-yl ester(CAS DataBase Reference)
NIST Chemistry Reference: Benzoic acid (2R,3R,6S)-4-(tert-butyl-dimethyl-silanyloxy)-2-furan-2-yl-6-methoxy-3,6-dihydro-2H-pyran-3-yl ester(118893-75-7)
EPA Substance Registry System: Benzoic acid (2R,3R,6S)-4-(tert-butyl-dimethyl-silanyloxy)-2-furan-2-yl-6-methoxy-3,6-dihydro-2H-pyran-3-yl ester(118893-75-7)

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: 118893-75-7(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 118893-75-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,8,8,9 and 3 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 118893-75:
(8*1)+(7*1)+(6*8)+(5*8)+(4*9)+(3*3)+(2*7)+(1*5)=167
167 % 10 = 7
So 118893-75-7 is a valid CAS Registry Number.

118893-75-7Upstream product

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118893-75-7Relevant academic research and scientific papers

A Stereoselective Totally Synthetic Route to Methyl α-Peracetylhikosaminide

Danishefsky, Samuel J.,Maring, Clarence J.

, p. 2193 - 2204 (2007/10/02)

A synthesis of the title system from D-galactose has been achieved.The racemic galactose 1,2,3,4-bisacetonide is expanded to a C7 heptulose, which is then extended to an undecose by a Lewis acid catalyzed cyclocondensation reaction.Racemic galactose was s

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