Cas 934480-58-7,(4S,5R)-bis-isobutyryloxy-(6S)-(2-phenylethyloxy)-tetrahydropyran-(2S)-carboxylic acid methyl ester

934480-58-7

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Basic information

Product Name: (4S,5R)-bis-isobutyryloxy-(6S)-(2-phenylethyloxy)-tetrahydropyran-(2S)-carboxylic acid methyl ester
Synonyms: (4S,5R)-bis-isobutyryloxy-(6S)-(2-phenylethyloxy)-tetrahydropyran-(2S)-carboxylic acid methyl ester
CAS NO:934480-58-7
Molecular Formula:
Molecular Weight: 436.502
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: (4S,5R)-bis-isobutyryloxy-(6S)-(2-phenylethyloxy)-tetrahydropyran-(2S)-carboxylic acid methyl ester(CAS DataBase Reference)
NIST Chemistry Reference: (4S,5R)-bis-isobutyryloxy-(6S)-(2-phenylethyloxy)-tetrahydropyran-(2S)-carboxylic acid methyl ester(934480-58-7)
EPA Substance Registry System: (4S,5R)-bis-isobutyryloxy-(6S)-(2-phenylethyloxy)-tetrahydropyran-(2S)-carboxylic acid methyl ester(934480-58-7)

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: 934480-58-7(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 934480-58-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,3,4,4,8 and 0 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 934480-58:
(8*9)+(7*3)+(6*4)+(5*4)+(4*8)+(3*0)+(2*5)+(1*8)=187
187 % 10 = 7
So 934480-58-7 is a valid CAS Registry Number.

934480-58-7Upstream product

934480-58-7Downstream Products

934480-58-7Relevant academic research and scientific papers

Convenient syntheses of deoxypyranose sugars from glucuronolactone

Stanford (nee Sinnott), Deborah,Stachulski, Andrew V.

, p. 2361 - 2364 (2007)

One of the characteristic reactions of glucuronic acid derivatives is the base-catalysed elimination of a 4-(substituted) hydroxy group to generate a Δ4,5 pyranose. Following hydrogenation, proceeding mainly from the α-face provided the anomeri

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