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1H-Indole-3-methanimine, N-(5-chloro-4-pentenyl)-1-[(4-methoxyphenyl)sulfonyl]-2-methyl-, (E,E)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

84960-65-6

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84960-65-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 84960-65-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,4,9,6 and 0 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 84960-65:
(7*8)+(6*4)+(5*9)+(4*6)+(3*0)+(2*6)+(1*5)=166
166 % 10 = 6
So 84960-65-6 is a valid CAS Registry Number.

84960-65-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name (E)-1-<(p-methoxyphenyl)sulfonyl>-2-methyl-3-<N-((E)-5-chloro-4-penten-1-yl)formimidoyl>indole

1.2 Other means of identification

Product number -
Other names (E)-1-[(p-methoxyphenyl)sulfonyl]-2-methyl-3-[N-((E)-5-chloro-4-penten-1-yl)formimidoyl]indole

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:84960-65-6 SDS

84960-65-6Downstream Products

84960-65-6Relevant academic research and scientific papers

Synthesis of (+/-)-10,22-Dioxokopsane and (+/-)-Kopsanone, Heptacyclic Indole Alkaloids. Synthetic and Mechanistic Studies

Magnus, Philip,Gallagher, Timothy,Brown, Peter,Huffman, John C.

, p. 2105 - 2114 (2007/10/02)

The total synthesis of the heptacyclic indole alkaloids (+/-)-10,22-dioxokopsane (2) and (+/-)-kopsanone (3, X=O) is described.The imine 20 was condensed with β,β,β-trichloroethyl chloroformate to give the tetracyclic carbamate 21.Removal of the carbamate

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