Cas 1241380-57-3,p-methoxyphenyl 6-O-tert-butyldiphenylsilyl-2,3-dideoxy-α-D-glycelo-hex-2-enopyranos-4-uloside

1241380-57-3

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Basic information

Product Name: p-methoxyphenyl 6-O-tert-butyldiphenylsilyl-2,3-dideoxy-α-D-glycelo-hex-2-enopyranos-4-uloside
Synonyms: p-methoxyphenyl 6-O-tert-butyldiphenylsilyl-2,3-dideoxy-α-D-glycelo-hex-2-enopyranos-4-uloside
CAS NO:1241380-57-3
Molecular Formula:
Molecular Weight: 488.656
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: p-methoxyphenyl 6-O-tert-butyldiphenylsilyl-2,3-dideoxy-α-D-glycelo-hex-2-enopyranos-4-uloside(CAS DataBase Reference)
NIST Chemistry Reference: p-methoxyphenyl 6-O-tert-butyldiphenylsilyl-2,3-dideoxy-α-D-glycelo-hex-2-enopyranos-4-uloside(1241380-57-3)
EPA Substance Registry System: p-methoxyphenyl 6-O-tert-butyldiphenylsilyl-2,3-dideoxy-α-D-glycelo-hex-2-enopyranos-4-uloside(1241380-57-3)

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: 1241380-57-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1241380-57-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,4,1,3,8 and 0 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1241380-57:
(9*1)+(8*2)+(7*4)+(6*1)+(5*3)+(4*8)+(3*0)+(2*5)+(1*7)=123
123 % 10 = 3
So 1241380-57-3 is a valid CAS Registry Number.

1241380-57-3Upstream product

1241380-56-2 p-methoxyphenyl 6-O-tert-butyldiphenylsilyl-α-D-erythro-hex-2-enopyranoside

1241380-57-3Downstream Products

1241380-58-4 6-O-tert-butyldiphenylsilyl-2,3-dideoxy-α-D-glycelo-hex-2-enopyranos-4-ulose

1241380-57-3Relevant academic research and scientific papers

Effective and chemoselective glycosylations using 2,3-unsaturated sugars

Kusumi, Shunichi,Sasaki, Kaname,Wang, Sainan,Watanabe, Tatsuya,Takahashi, Daisuke,Toshima, Kazunobu

supporting information; experimental part, p. 3164 - 3178 (2010/08/21)

Glycosyl donors containing a double bond between C2 and C3 were designed by mimicking the reaction mechanism of lysozyme-initiated hydrolysis of mucopolysaccharides. It was found that, under various glycosylation conditions, the reactivities of 2,3-unsatu

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