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626-21-1

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626-21-1 Usage

Physical Properties

Appearance: Colorless to pale yellow liquid
Odor: Pungent

Primary Uses

Intermediate in the manufacture of agricultural and pharmaceutical products

Derivative

Derivative of pyridine

Synthetic Applications

Building block in the synthesis of various organic compounds
Catalyst in organic reactions

Commercial Importance

Limited commercial uses on its own but plays a significant role in the production of other chemical products

Safety Considerations

Should be handled with caution
Harmful if it comes into contact with skin, eyes, or if inhaled or ingested.

Check Digit Verification of cas no

The CAS Registry Mumber 626-21-1 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 6,2 and 6 respectively; the second part has 2 digits, 2 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 626-21:
(5*6)+(4*2)+(3*6)+(2*2)+(1*1)=61
61 % 10 = 1
So 626-21-1 is a valid CAS Registry Number.

626-21-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,4-diethylpyridine

1.2 Other means of identification

Product number -
Other names Pyridine,2,4-diethyl

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:626-21-1 SDS

626-21-1Downstream Products

626-21-1Relevant articles and documents

Electron and Hydrogen Transfer Reductions of Some 2,4-Disubstituted Pyridines

Attia, A.,El-Salam, O. I. Abd,Youssef, T. E.

, p. 351 - 362 (2007/10/03)

New synthesis of 2,4-diacetylpyridine 1 was undertaken by Claisen condensation of 2,4-diethoxycarbonylpyridine 2a with ethyl acetate, followed by hydrolysis of the intermediate 3. Reduction of 1 with zinc or its salt in hydrochloric, formic or acetic acids afforded mixtures of the ketocarbinol 4 dicarbinol 5 or diethyl 6 pyridine derivatives. Formation of 6 as the complete reduction product was chemically proved to proceed via 4 and 5. Electrochemical reduction of 2a leads to 2,4-dimethylpyridine 7, and that of 1 gave rise to a mixture of 5 and 6 along with 2,4-diethyl-1,2,5,6-tetrahydropyridine 8 and 2,4-diethylpiperidine 9. Finally, metal hydride reduction of 1 gave 5, and that of diesters 2 or diacid chloride 10 derivatives afforded 2,4-dihydroxymethylpyridine 11.

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