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365261-27-4

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365261-27-4 Usage

General Description

3-Bromo-1-methyl-1,2,5,6-tetrahydropyridine is a chemical compound with the molecular formula C6H10BrN. It is an organic compound that contains a bromine atom and a methyl group attached to a tetrahydropyridine ring. This chemical is commonly used in organic synthesis and pharmaceutical research as it serves as a versatile building block for various compounds. It is also utilized in the production of certain drugs and agrochemicals. Additionally, 3-Bromo-1-methyl-1,2,5,6-tetrahydropyridine may have potential applications in the field of neuroscience and neuropharmacology due to its structural similarity to certain neurotransmitters and its potential effects on the central nervous system.

Check Digit Verification of cas no

The CAS Registry Mumber 365261-27-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,6,5,2,6 and 1 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 365261-27:
(8*3)+(7*6)+(6*5)+(5*2)+(4*6)+(3*1)+(2*2)+(1*7)=144
144 % 10 = 4
So 365261-27-4 is a valid CAS Registry Number.

365261-27-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-Bromo-1-methyl-1,2,5,6-tetrahydropyridine

1.2 Other means of identification

Product number -
Other names 5-bromo-1-methyl-3,6-dihydro-2H-pyridine

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:365261-27-4 SDS

365261-27-4Relevant articles and documents

Method for synthesizing N-substitute-1, 2, 3, 6-tetrahydropyridine-5-boric acid ester

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Paragraph 0017, (2016/11/07)

The invention discloses a method for synthesizing N-substitute-1, 2, 3, 6-tetrahydropyridine-5-boric acid ester. According to the method, N-substitute-1, 2, 3, 6-tetrahydropyridine-5-carboxylic acid (ester) serves as the raw material, conducts addition with halogen and then is subjected to alkaline condition elimination to form alkenyl halide and then subjected to coupling with al boron ester under the condition of metal palladium catalyzation, and the N-substitute-1, 2, 3, 6-tetrahydropyridine-5-boric acid ester is obtained. According to the method, the obtained midbody alkenyl halide does not contain isomer, separation is easy to conduct, purity of an obtained product is high, and the method provides a simple way for synthesis of compounds of the type.

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