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100289-21-2

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100289-21-2 Usage

Class

Skeletal muscle relaxants

Use

Treat musculoskeletal pain and discomfort associated with strains, sprains, and other muscle injuries

Mechanism of Action

Acts on the central nervous system to produce muscle relaxation and relieve pain

Administration

Orally in tablet form

Additional Treatment

May be prescribed in combination with physical therapy and rest

Tolerance

Generally well-tolerated

Common Side Effects

Drowsiness, dizziness, and nausea

Precautions

Avoid consuming alcohol and operating heavy machinery due to potential for increased drowsiness and impaired cognition

Efficacy

Effective and commonly prescribed medication for the relief of acute musculoskeletal pain

Check Digit Verification of cas no

The CAS Registry Mumber 100289-21-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,0,2,8 and 9 respectively; the second part has 2 digits, 2 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 100289-21:
(8*1)+(7*0)+(6*0)+(5*2)+(4*8)+(3*9)+(2*2)+(1*1)=82
82 % 10 = 2
So 100289-21-2 is a valid CAS Registry Number.

100289-21-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 10, 2017

Revision Date: Aug 10, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(2-Methylimidazo[1,2-a]pyrimidin-3-yl)ethanon

1.2 Other means of identification

Product number -
Other names 1-(2-Methyl-imidazo[1,2-a]pyrimidin-3-yl)-ethanone

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:100289-21-2 SDS

100289-21-2Relevant articles and documents

Therapeutic compounds

-

Page/Page column 15; 25; 26, (2021/01/17)

The invention provides a compound of formula I: or a salt thereof, wherein R2-R4 and p have any of the values described in the specification, as well as compositions comprising a compound of formula I. The compounds are useful as ant

Hypervalent iodine(III) promoted direct synthesis of imidazo[1,2-a] pyrimidines

Qian, Guangyin,Liu, Bingxin,Tan, Qitao,Zhang, Siwen,Xu, Bin

, p. 4837 - 4843 (2014/08/05)

An efficient and mild synthesis of imidazo[1,2-a]pyrimidine derivatives has been developed from readily available pyrimidyl arylamines or enamines through a hypervalent iodine-promoted intramolecular C-H bond cycloamination reaction. This protocol allows for the facile construction of biologically active bicyclic imidazo[1,2-a]pyrimidine skeletons as well as other imidazo[1,2-a]-type fused heterocycles.

BMI-1 PROTEIN EXPRESSION MODULATORS

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Page/Page column 84, (2010/04/03)

The compounds, pharmaceutical compositions, and methods of using such compounds or compositions thereof described herein are useful for treating a disease modulated by B-cell specific Moloney murine leukemia virus integration site 1 (Bmi-1) protein expression.

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