Cas 1225450-79-2,allyl (methyl 2,3-di-O-(4-methoxyphenylmethyl)-4-O-trifluoromethanesulfonyl-α-D-glucopyranosid)uronate

1225450-79-2

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Basic information

Product Name: allyl (methyl 2,3-di-O-(4-methoxyphenylmethyl)-4-O-trifluoromethanesulfonyl-α-D-glucopyranosid)uronate
Synonyms: allyl (methyl 2,3-di-O-(4-methoxyphenylmethyl)-4-O-trifluoromethanesulfonyl-α-D-glucopyranosid)uronate
CAS NO:1225450-79-2
Molecular Formula:
Molecular Weight: 620.598
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: allyl (methyl 2,3-di-O-(4-methoxyphenylmethyl)-4-O-trifluoromethanesulfonyl-α-D-glucopyranosid)uronate(CAS DataBase Reference)
NIST Chemistry Reference: allyl (methyl 2,3-di-O-(4-methoxyphenylmethyl)-4-O-trifluoromethanesulfonyl-α-D-glucopyranosid)uronate(1225450-79-2)
EPA Substance Registry System: allyl (methyl 2,3-di-O-(4-methoxyphenylmethyl)-4-O-trifluoromethanesulfonyl-α-D-glucopyranosid)uronate(1225450-79-2)

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: 1225450-79-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1225450-79-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,2,5,4,5 and 0 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1225450-79:
(9*1)+(8*2)+(7*2)+(6*5)+(5*4)+(4*5)+(3*0)+(2*7)+(1*9)=132
132 % 10 = 2
So 1225450-79-2 is a valid CAS Registry Number.

1225450-79-2Upstream product

1225450-79-2Downstream Products

1225450-80-5 C₁₁₇H₁₂₀O₂₂S

1225450-79-2Relevant academic research and scientific papers

Synthesis of a trigalacturonic acid analogue mimicking the expected transition state in the glycosidases

Yamamoto, Kazunori,Noguchi, Shogo,Takada, Noboru,Miyairi, Kazuo,Hashimoto, Masaru

, p. 572 - 585 (2010)

A trigalacturonic acid analogue carrying a cyclohexene framework in place of the central pyranose ring was synthesized as a molecular probe for the mechanistic investigation of endo-polygalacturonase 1 (endo-PG 1). Preliminary enzymatic studies revealed t

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