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207451-81-8

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207451-81-8 Usage

General Description

7-Methyl-1,2,3,4-tetrahydro-isoquinoline is a chemical compound with a molecular formula C10H13N. It is a derivative of isoquinoline and consists of a six-membered ring fused to a five-membered ring. 7-METHYL-1,2,3,4-TETRAHYDRO-ISOQUINOLINE is found in a variety of natural products including plants and animals. It has been studied for its potential biological activities, including its role as a neurotransmitter and its potential as an analgesic. Additionally, 7-Methyl-1,2,3,4-tetrahydro-isoquinoline has been investigated for its potential as a precursor in the synthesis of pharmaceutical compounds and other organic molecules.

Check Digit Verification of cas no

The CAS Registry Mumber 207451-81-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,0,7,4,5 and 1 respectively; the second part has 2 digits, 8 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 207451-81:
(8*2)+(7*0)+(6*7)+(5*4)+(4*5)+(3*1)+(2*8)+(1*1)=118
118 % 10 = 8
So 207451-81-8 is a valid CAS Registry Number.
InChI:InChI=1/C10H13N/c1-8-2-3-9-4-5-11-7-10(9)6-8/h2-3,6,11H,4-5,7H2,1H3

207451-81-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 7-Methyl-1,2,3,4-tetrahydroisoquinoline hydrochloride

1.2 Other means of identification

Product number -
Other names 7-methyl-1,2,3,4-tetrahydroisoquinoline

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:207451-81-8 SDS

207451-81-8Relevant articles and documents

Catalyst-free cyclization of anthranils and cyclic amines: One-step synthesis of rutaecarpine

Li, Jian,Wang, Zheng-Bing,Xu, Yue,Lu, Xue-Chen,Zhu, Shang-Rong,Liu, Li

supporting information, p. 12072 - 12075 (2019/10/14)

An efficient synthesis of a variety of quinazolinone derivatives via a direct cyclization reaction between commercially available anthranils and cyclic amines is described. The developed transformation proceeds with the merits of high step- and atom-efficiency, a broad substrate scope, and good to excellent yields, without additional catalysts, and offers a practical way for the preparation of rutaecarpine and its derivatives with structural diversity.

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