Cas 176787-45-4,Imidazole-1-carboxylic acid (2R,3R,4S,5R,6S)-4,5-bis-benzyloxy-2-benzyloxymethyl-6-methoxy-tetrahydro-pyran-3-yl ester

176787-45-4

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Basic information

Product Name: Imidazole-1-carboxylic acid (2R,3R,4S,5R,6S)-4,5-bis-benzyloxy-2-benzyloxymethyl-6-methoxy-tetrahydro-pyran-3-yl ester
Synonyms: Imidazole-1-carboxylic acid (2R,3R,4S,5R,6S)-4,5-bis-benzyloxy-2-benzyloxymethyl-6-methoxy-tetrahydro-pyran-3-yl ester
CAS NO:176787-45-4
Molecular Formula:
Molecular Weight: 558.631
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: Imidazole-1-carboxylic acid (2R,3R,4S,5R,6S)-4,5-bis-benzyloxy-2-benzyloxymethyl-6-methoxy-tetrahydro-pyran-3-yl ester(CAS DataBase Reference)
NIST Chemistry Reference: Imidazole-1-carboxylic acid (2R,3R,4S,5R,6S)-4,5-bis-benzyloxy-2-benzyloxymethyl-6-methoxy-tetrahydro-pyran-3-yl ester(176787-45-4)
EPA Substance Registry System: Imidazole-1-carboxylic acid (2R,3R,4S,5R,6S)-4,5-bis-benzyloxy-2-benzyloxymethyl-6-methoxy-tetrahydro-pyran-3-yl ester(176787-45-4)

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: 176787-45-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 176787-45-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,6,7,8 and 7 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 176787-45:
(8*1)+(7*7)+(6*6)+(5*7)+(4*8)+(3*7)+(2*4)+(1*5)=194
194 % 10 = 4
So 176787-45-4 is a valid CAS Registry Number.

176787-45-4Upstream product

176787-45-4Downstream Products

205518-27-0 Carbonic acid (2R,3R,4S,5R,6S)-4,5-bis-benzyloxy-2-benzyloxymethyl-6-methoxy-tetrahydro-pyran-3-yl ester (3R,4S,5S,6R)-3,4,5-tris-benzyloxy-6-benzyloxymethyl-tetrahydro-pyran-2-yl ester

176787-45-4Relevant academic research and scientific papers

A novel intramolecular decarboxylative glycosylation via mixed carbonate

Iimori, Takamasa,Shibazaki, Takafumi,Ikegami, Shiro

, p. 2267 - 2270 (1996)

A two-step glycosylation procedure, which involves (1) linking two sugars by using carbonate as a connector, (2) removing carbon dioxide to form a glycosidic bond by the aid of Lewis acid, has been developed. This glycosylation procedure was based on the opposite mode of connection, where a glycosyl acceptor was activated to link sugars.

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