Cas 178152-66-4,Acetic acid (1S,2R,3S,4R,5R,6R)-3,4-dihydroxy-2,5,6-tris-phosphonooxy-cyclohexyl ester

178152-66-4

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Basic information

Product Name: Acetic acid (1S,2R,3S,4R,5R,6R)-3,4-dihydroxy-2,5,6-tris-phosphonooxy-cyclohexyl ester
Synonyms: Acetic acid (1S,2R,3S,4R,5R,6R)-3,4-dihydroxy-2,5,6-tris-phosphonooxy-cyclohexyl ester
CAS NO:178152-66-4
Molecular Formula:
Molecular Weight: 462.135
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: Acetic acid (1S,2R,3S,4R,5R,6R)-3,4-dihydroxy-2,5,6-tris-phosphonooxy-cyclohexyl ester(CAS DataBase Reference)
NIST Chemistry Reference: Acetic acid (1S,2R,3S,4R,5R,6R)-3,4-dihydroxy-2,5,6-tris-phosphonooxy-cyclohexyl ester(178152-66-4)
EPA Substance Registry System: Acetic acid (1S,2R,3S,4R,5R,6R)-3,4-dihydroxy-2,5,6-tris-phosphonooxy-cyclohexyl ester(178152-66-4)

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: 178152-66-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 178152-66-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,8,1,5 and 2 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 178152-66:
(8*1)+(7*7)+(6*8)+(5*1)+(4*5)+(3*2)+(2*6)+(1*6)=154
154 % 10 = 4
So 178152-66-4 is a valid CAS Registry Number.

178152-66-4Upstream product

6763-47-9 rac-1,2-O-cyclohexylidene-myo-inositol

178152-66-4Downstream Products

178152-66-4Relevant academic research and scientific papers

Lipase-catalyzed regio- and enantioselective esterification of rac-1,2-O-cyclohexylidene-myo-inositol

Rudolf, Marco T.,Schultz, Carsten

, p. 533 - 537 (2007/10/03)

The hydroxyl group at C-5 in racemic 1,2-O-Cyclohexylidene-myo-inositol (rac-1) was regio- and enantioselectively acylated to give 5-O-acetyl- (2a)- or 5-O-butyryl-2,3-O-cyclohexylidene-myo-inositol (3a), respectively, by treatment of 1 with vinyl acetate

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