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1007089-84-0

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1007089-84-0 Usage

Uses

3-Chloromethyl-5-methylpyridine is an intermediate in the synthesis of Rupatadine (R701650).

Check Digit Verification of cas no

The CAS Registry Mumber 1007089-84-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,0,7,0,8 and 9 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1007089-84:
(9*1)+(8*0)+(7*0)+(6*7)+(5*0)+(4*8)+(3*9)+(2*8)+(1*4)=130
130 % 10 = 0
So 1007089-84-0 is a valid CAS Registry Number.

1007089-84-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-(Chloromethyl)-5-methylpyridine hydrochloride

1.2 Other means of identification

Product number -
Other names 3-Chloromethyl-5-methylpyridine Hydrochloride

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:1007089-84-0 SDS

1007089-84-0Downstream Products

1007089-84-0Relevant articles and documents

Expedient synthesis of rupatadine

Agarwal, Rajendra,Bhirud, Shekhar Bhaskar,Bijukumar, Gopinathenpillai,Khude, Gopal Dnyandev

, p. 122 - 127 (2008)

Rupatadine, a new potent, orally active dual antagonist of histamine and platelet-activating factor (PAF), has been synthesized in 91% overall yield. Copyright Taylor & Francis Group, LLC.

Preparation process of Rupatadine

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Paragraph 0056; 0062; 0068; 0074; 0080; 0086; 0092; 0096, (2017/08/28)

The invention discloses a rupatadine preparation process, which comprises: S1, preparing methyl 5-methylnicotinate; S2, preparing 5-methyl-3-pyridinemethanol; S3, preparing 3-methyl-5-chloromethylpyridine hydrochloride; and S4, preparing rupatadine. According to the present invention, the preparation process has advantages of low cost, mild reaction condition, simple operation, low requirement onequipment, good product purity and high yield, and is suitable for large-scale industrial production.

4H- [1, 2, 4] TRIAZOLO [5, 1 -B] PYRIMIDIN-7 -ONE DERIVATIVES AS CCR2B RECEPTOR ANTAGONISTS

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Page/Page column 86, (2011/10/10)

The present invention relates to novel compounds for use in the compositions, to processes for their preparation, to intermediates useful in their preparation and to their use as therapeutic agents. The present invention also relates to pharmaceutical com

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