Cas 888012-98-4,phenyl 2,3-di-O-acetyl-4-O-chloroacetyl-6-O-tert-butyldimethylsilyl-1-thio-β-D-glucopyranoside

888012-98-4

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Basic information

Product Name: phenyl 2,3-di-O-acetyl-4-O-chloroacetyl-6-O-tert-butyldimethylsilyl-1-thio-β-D-glucopyranoside
Synonyms: phenyl 2,3-di-O-acetyl-4-O-chloroacetyl-6-O-tert-butyldimethylsilyl-1-thio-β-D-glucopyranoside
CAS NO:888012-98-4
Molecular Formula:
Molecular Weight: 547.142
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: phenyl 2,3-di-O-acetyl-4-O-chloroacetyl-6-O-tert-butyldimethylsilyl-1-thio-β-D-glucopyranoside(CAS DataBase Reference)
NIST Chemistry Reference: phenyl 2,3-di-O-acetyl-4-O-chloroacetyl-6-O-tert-butyldimethylsilyl-1-thio-β-D-glucopyranoside(888012-98-4)
EPA Substance Registry System: phenyl 2,3-di-O-acetyl-4-O-chloroacetyl-6-O-tert-butyldimethylsilyl-1-thio-β-D-glucopyranoside(888012-98-4)

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: 888012-98-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 888012-98-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,8,8,0,1 and 2 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 888012-98:
(8*8)+(7*8)+(6*8)+(5*0)+(4*1)+(3*2)+(2*9)+(1*8)=204
204 % 10 = 4
So 888012-98-4 is a valid CAS Registry Number.

888012-98-4Upstream product

79-04-9 chloroacetyl chloride

888012-98-4Downstream Products

888012-98-4Relevant academic research and scientific papers

A novel and efficient ionic liquid supported synthesis of oligosaccharides

Huang, Jian-Ying,Lei, Ming,Wang, Yan-Guang

, p. 3047 - 3050 (2006)

A novel and efficient ionic liquid supported synthesis of oligosaccharides with a general protocol of coupling and purification is described. The method represents an attractive alternative to the classical solid- and fluorous-phase synthesis strategies a

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