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phendimetrazine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

21784-30-5

21784-30-5 Suppliers

This product is a nationally controlled contraband or patented product, and the Lookchem platform doesn't provide relevant sales information.

21784-30-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 21784-30-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,1,7,8 and 4 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 21784-30:
(7*2)+(6*1)+(5*7)+(4*8)+(3*4)+(2*3)+(1*0)=105
105 % 10 = 5
So 21784-30-5 is a valid CAS Registry Number.
InChI:InChI=1/C12H17NO.ClH/c1-10-12(14-9-8-13(10)2)11-6-4-3-5-7-11;/h3-7,10,12H,8-9H2,1-2H3;1H

21784-30-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name Phendimetrazine

1.2 Other means of identification

Product number -
Other names phendimetrazine

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:21784-30-5 SDS

21784-30-5Relevant academic research and scientific papers

Facile, efficient, and catalyst-free electrophilic aminoalkoxylation of olefins: Scope and application

Zhou, Ling,Tan, Chong Kiat,Zhou, Jing,Yeung, Ying-Yeung

supporting information; experimental part, p. 10245 - 10247 (2010/09/07)

A new one-pot electrophilic aminoalkoxylation reaction using olefin, cyclic ether, amine, and N-bromosuccinimide has been developed. The olefinic substrates and the cyclic ether partners can be flexibly varied to produce a range of amino ether derivatives. This novel protocol has been applied in the facile and efficient synthesis of biologically active morpholine compounds.