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211871-49-7

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211871-49-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 211871-49-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,1,1,8,7 and 1 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 211871-49:
(8*2)+(7*1)+(6*1)+(5*8)+(4*7)+(3*1)+(2*4)+(1*9)=117
117 % 10 = 7
So 211871-49-7 is a valid CAS Registry Number.

211871-49-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-methyl-1-naphthalen-1-ylpropan-2-amine

1.2 Other means of identification

Product number -
Other names A,A-DIMETHYL-1-NAPHTHALENEETHANAMINE

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:211871-49-7 SDS

211871-49-7Downstream Products

211871-49-7Relevant articles and documents

Photoamination of Alkenylnaphthalenes with Ammonia via Electron Transfer

Yasuda, Masahide,Kojima, Ryuji,Ohira, Ryujiro,Shiragami, Tsutomu,Shima, Kensuke

, p. 1655 - 1660 (2007/10/03)

The photoamination of l-(2-methyl-l-propenyl)naphthalene (1a) with ammonia in the presence of p-dicyanobenzene (p-DCB) occurred selectively at the alkenyl group but not at the naphthyl group to give l-(2-amino-2-methylpropyl)naphthalene (2a). Similarly, the photoamination of several kinds of alkenylnaphthalenes (1) proceeded selectively at the alkenyl group. The photoamination proceeded via the nucleophilic addition of ammonia to the cation radical of 1 generated by the photoinduced electron transfer to p-DCB to give the aminated radical after deprotonation. Distribution of the positive charge in 1+· and the stabilities of the aminated radicals were calculated by the PM3-UHF method. The stabilities of the aminated radicals agreed with the regioselectivity.

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