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1384265-30-8

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1384265-30-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1384265-30-8 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,8,4,2,6 and 5 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1384265-30:
(9*1)+(8*3)+(7*8)+(6*4)+(5*2)+(4*6)+(3*5)+(2*3)+(1*0)=168
168 % 10 = 8
So 1384265-30-8 is a valid CAS Registry Number.

1384265-30-8SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name methyl 1-(4-bromophenyl)-4-oxocyclohexane-1-carboxylate

1.2 Other means of identification

Product number -
Other names -

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:1384265-30-8 SDS

1384265-30-8Relevant articles and documents

Successful strategies for mitigation of a preclinical signal for phototoxicity in a dgat1 inhibitor

Harrison, Tyler J.,Bauer, Daniel,Berdichevsky, Alina,Chen, Xin,Duvadie, Rohit,Hoogheem, Benjamin,Hatsis, Panos,Liu, Qian,Mao, Justin,Miduturu, Vasumathy,Rocheford, Erik,Zecri, Frederic,Zessis, Richard,Zheng, Rui,Zhu, Qingming,Streeper, Ryan,Patel, Sejal J.

, p. 1128 - 1133 (2019/08/27)

Diacylglycerol O-acyltransferase 1 (DGAT1) inhibitor Pradigastat (1) was shown to be effective at decreasing postprandial triglyceride levels in a patient population with familial chylomicronemia syndrome (FCS). Although pradigastat does not cause photosensitization in humans at the high clinical dose of 40 mg, a positive signal was observed in preclinical models of phototoxicity. Herein, we describe a preclinical phototoxicity mitigation strategy for diarylamine containing molecules utilizing the introduction of an amide or suitable heterocyclic function. This strategy led to the development of two second-generation compounds with low risk of phototoxicity, disparate exposure profiles, and comparable efficacy to 1 in a rodent lipid bolus model for post-prandial plasma triglycerides.

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