Cas 1323988-33-5,(1S)-1,5-anhydro-2-deoxy-1-(2,6-dimethoxyphenyl)-3,4,6-tris-O-(phenylmethyl)-D-erythro-hex-2-enitol

1323988-33-5

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Basic information

Product Name: (1S)-1,5-anhydro-2-deoxy-1-(2,6-dimethoxyphenyl)-3,4,6-tris-O-(phenylmethyl)-D-erythro-hex-2-enitol
Synonyms: (1S)-1,5-anhydro-2-deoxy-1-(2,6-dimethoxyphenyl)-3,4,6-tris-O-(phenylmethyl)-D-erythro-hex-2-enitol
CAS NO:1323988-33-5
Molecular Formula:
Molecular Weight: 552.667
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: (1S)-1,5-anhydro-2-deoxy-1-(2,6-dimethoxyphenyl)-3,4,6-tris-O-(phenylmethyl)-D-erythro-hex-2-enitol(CAS DataBase Reference)
NIST Chemistry Reference: (1S)-1,5-anhydro-2-deoxy-1-(2,6-dimethoxyphenyl)-3,4,6-tris-O-(phenylmethyl)-D-erythro-hex-2-enitol(1323988-33-5)
EPA Substance Registry System: (1S)-1,5-anhydro-2-deoxy-1-(2,6-dimethoxyphenyl)-3,4,6-tris-O-(phenylmethyl)-D-erythro-hex-2-enitol(1323988-33-5)

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: 1323988-33-5(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1323988-33-5 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,2,3,9,8 and 8 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1323988-33:
(9*1)+(8*3)+(7*2)+(6*3)+(5*9)+(4*8)+(3*8)+(2*3)+(1*3)=175
175 % 10 = 5
So 1323988-33-5 is a valid CAS Registry Number.

1323988-33-5Upstream product

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1323988-33-5Relevant academic research and scientific papers

Regio- and stereoselective synthesis of 2-deoxy-C-aryl glycosides via palladium catalyzed decarboxylative reactions

Xiang, Shaohua,Cai, Shuting,Zeng, Jing,Liu, Xue-Wei

, p. 4608 - 4611 (2011)

An efficient and versatile approach for the synthesis of 2-deoxy-C-aryl glycosides is reported. This strategy is based on a palladium-catalyzed decarboxylative Heck coupling reaction of benzoic acids and glycals. A wide variety of glycals and benzoic acid

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