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23000-11-5

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23000-11-5 Usage

Physical form

Yellow crystalline solid

Uses

Metabolic uncoupler in biochemical research, pesticide

Mechanism of action

Disrupts oxidative phosphorylation in mitochondria, leading to dissipation of proton gradient and production of heat instead of ATP

Effects on body

Induces weight loss and increases metabolic rate

Toxicity

Significant, with potential for severe side effects including hyperthermia, organ failure, and death

Legal status

Not approved for human consumption or use

Check Digit Verification of cas no

The CAS Registry Mumber 23000-11-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,3,0,0 and 0 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 23000-11:
(7*2)+(6*3)+(5*0)+(4*0)+(3*0)+(2*1)+(1*1)=35
35 % 10 = 5
So 23000-11-5 is a valid CAS Registry Number.

23000-11-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,4-dimethyl-5-(4-nitrophenyl)-1,3-oxazole

1.2 Other means of identification

Product number -
Other names 2,4-Dimethyl-5-(p-phenyl)-oxazol

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:23000-11-5 SDS

23000-11-5Relevant articles and documents

Inhibitors of inosine monophosphate dehydrogenase: SARs about the N-[3-methoxy-4-(5-oxazolyl)phenyl moiety

Iwanowicz, Edwin J.,Watterson, Scott H.,Guo, Junqing,Pitts, William J.,Murali Dhar,Shen, Zhongqi,Chen, Ping,Gu, Henry H.,Fleener, Catherine A.,Rouleau, Katherine A.,Cheney, Daniel L.,Townsend, Robert M.,Hollenbaugh, Diane L.

, p. 2059 - 2063 (2007/10/03)

The first reported structure-activity relationships (SARs) about the N-[3-methoxy-4-(5-oxazolyl)phenyl moiety for a series of recently disclosed inosine monophosphate dehydrogenase (IMPDH) inhibitors are described. The syntheses and in vitro inhibitory values for IMPDH II, and T-cell proliferation (for select analogues) are given.

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