Cas 142200-26-8,Methyl-4-<(1S)-(1,4,6/5)-4,5,6-trihydroxy-3-hydroxymethyl-2-cyclohexen-1-yl>amino-D-glucopyranosid

142200-26-8

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Basic information

Product Name: Methyl-4-<(1S)-(1,4,6/5)-4,5,6-trihydroxy-3-hydroxymethyl-2-cyclohexen-1-yl>amino-D-glucopyranosid
Synonyms: Methyl-4-<(1S)-(1,4,6/5)-4,5,6-trihydroxy-3-hydroxymethyl-2-cyclohexen-1-yl>amino-D-glucopyranosid
CAS NO:142200-26-8
Molecular Formula:
Molecular Weight: 335.354
EINECS: N/A
Product Categories: N/A
Mol File: 142200-26-8.mol
Article Data: 1

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: Methyl-4-<(1S)-(1,4,6/5)-4,5,6-trihydroxy-3-hydroxymethyl-2-cyclohexen-1-yl>amino-D-glucopyranosid(CAS DataBase Reference)
NIST Chemistry Reference: Methyl-4-<(1S)-(1,4,6/5)-4,5,6-trihydroxy-3-hydroxymethyl-2-cyclohexen-1-yl>amino-D-glucopyranosid(142200-26-8)
EPA Substance Registry System: Methyl-4-<(1S)-(1,4,6/5)-4,5,6-trihydroxy-3-hydroxymethyl-2-cyclohexen-1-yl>amino-D-glucopyranosid(142200-26-8)

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: 142200-26-8(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 142200-26-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,2,2,0 and 0 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 142200-26:
(8*1)+(7*4)+(6*2)+(5*2)+(4*0)+(3*0)+(2*2)+(1*6)=68
68 % 10 = 8
So 142200-26-8 is a valid CAS Registry Number.

142200-26-8Upstream product

142200-26-8Downstream Products

80943-41-5 methyl 4-<<(1S,2S)-(2,4/3)-2,3,4-tetrahydroxy-5-(hydroxymethyl)-5-cyclohexen-1-yl>amino>-4,6-dideoxy-α-D-glucopyranoside

142200-26-8Relevant articles and documents

Synthesis and study of the pancreatic α-amylase inhibitory activity of methyl acarviosin and its derivatives

Kato, Eisuke,Chikahisa, Fumiaki,Kawabata, Jun

, p. 1365 - 1367 (2016)

Pancreatic α-amylase is a target for type 2 diabetes mellitus treatment. However, small molecule inhibitors of α-amylase are currently scarce. In the course of developing small molecule α-amylase inhibitors, we designed and synthesized conjugates of gluco

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