Cas 1058139-98-2,3,2-anhydro-6-p-methoxyphenyl-2-(3,4,6-tri-O-acetyl-β-D-mannopyranosyl)-3-mercapto-1,2,4-triazin-5(2H)-one

1058139-98-2

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Basic information

Product Name: 3,2-anhydro-6-p-methoxyphenyl-2-(3,4,6-tri-O-acetyl-β-D-mannopyranosyl)-3-mercapto-1,2,4-triazin-5(2H)-one
Synonyms: 3,2-anhydro-6-p-methoxyphenyl-2-(3,4,6-tri-O-acetyl-β-D-mannopyranosyl)-3-mercapto-1,2,4-triazin-5(2H)-one
CAS NO:1058139-98-2
Molecular Formula:
Molecular Weight: 505.505
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: 3,2-anhydro-6-p-methoxyphenyl-2-(3,4,6-tri-O-acetyl-β-D-mannopyranosyl)-3-mercapto-1,2,4-triazin-5(2H)-one(CAS DataBase Reference)
NIST Chemistry Reference: 3,2-anhydro-6-p-methoxyphenyl-2-(3,4,6-tri-O-acetyl-β-D-mannopyranosyl)-3-mercapto-1,2,4-triazin-5(2H)-one(1058139-98-2)
EPA Substance Registry System: 3,2-anhydro-6-p-methoxyphenyl-2-(3,4,6-tri-O-acetyl-β-D-mannopyranosyl)-3-mercapto-1,2,4-triazin-5(2H)-one(1058139-98-2)

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: 1058139-98-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1058139-98-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,5,8,1,3 and 9 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1058139-98:
(9*1)+(8*0)+(7*5)+(6*8)+(5*1)+(4*3)+(3*9)+(2*9)+(1*8)=162
162 % 10 = 2
So 1058139-98-2 is a valid CAS Registry Number.

1058139-98-2Upstream product

1058139-67-5 6-p-methoxyphenyl-2-(2,3,4,6-tetra-O-acetyl-β-D-glucopyranosyl)-2,3-dihydro-3-thioxo-1,2,4-triazin-5(4H)-one

1058139-98-2Downstream Products

1058139-98-2Relevant academic research and scientific papers

An improved direct synthetic approach to anhydronucleosides

Al-Juwaiser, Ibtehal A.,Ibrahim, Maher R.,Al-Awadi, Nouria A.,Ibrahim, Yehia A.

, p. 8206 - 8212 (2008)

The synthesis of anhydrothioglycosyls has been improved by studying the reaction under a variety of reaction conditions including gas phase pyrolysis, heating in a solvent of high boiling point, in the presence of different bases including triethylamine, DABCO, and DBU, and in a microwave reactor.

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