Cas 867262-98-4,2,6-diisopropylphenyl {[1-(2-methoxyphenyl)-4-(3-methoxyphenyl)piperidin-4-yl]carbonyl}sulfamate

867262-98-4

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Basic information

Product Name: 2,6-diisopropylphenyl {[1-(2-methoxyphenyl)-4-(3-methoxyphenyl)piperidin-4-yl]carbonyl}sulfamate
Synonyms: 2,6-diisopropylphenyl {[1-(2-methoxyphenyl)-4-(3-methoxyphenyl)piperidin-4-yl]carbonyl}sulfamate
CAS NO:867262-98-4
Molecular Formula:
Molecular Weight: 580.745
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: 2,6-diisopropylphenyl {[1-(2-methoxyphenyl)-4-(3-methoxyphenyl)piperidin-4-yl]carbonyl}sulfamate(CAS DataBase Reference)
NIST Chemistry Reference: 2,6-diisopropylphenyl {[1-(2-methoxyphenyl)-4-(3-methoxyphenyl)piperidin-4-yl]carbonyl}sulfamate(867262-98-4)
EPA Substance Registry System: 2,6-diisopropylphenyl {[1-(2-methoxyphenyl)-4-(3-methoxyphenyl)piperidin-4-yl]carbonyl}sulfamate(867262-98-4)

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: 867262-98-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 867262-98-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,6,7,2,6 and 2 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 867262-98:
(8*8)+(7*6)+(6*7)+(5*2)+(4*6)+(3*2)+(2*9)+(1*8)=214
214 % 10 = 4
So 867262-98-4 is a valid CAS Registry Number.

867262-98-4Upstream product

92050-02-7 sulfamate de diisopropyl-2,6 phenyle

867262-98-4Downstream Products

867262-98-4Relevant academic research and scientific papers

A novel class of antihyperlipidemic agents with low density lipoprotein receptor up-regulation via the adaptor protein autosomal recessive hypercholesterolemia

Asano, Shigehiro,Ban, Hitoshi,Tsuboya, Norie,Uno, Shinsaku,Kino, Kouichi,Ioriya, Katsuhisa,Kitano, Masafumi,Ueno, Yoshihide

experimental part, p. 3284 - 3295 (2010/09/05)

We have previously reported compound 2 as a inhibitor of acyl-coenzyme A:cholesterol O-acyltransferase (ACAT) and up-regulator of the low density lipoprotein receptor (LDL-R) expression. In this study we focused on compound 2, a unique LDL-R up-regulator,

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