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Methyl 2-(6-chloro-1H-indol-3-yl)acetate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

53859-25-9

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53859-25-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 53859-25-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,3,8,5 and 9 respectively; the second part has 2 digits, 2 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 53859-25:
(7*5)+(6*3)+(5*8)+(4*5)+(3*9)+(2*2)+(1*5)=149
149 % 10 = 9
So 53859-25-9 is a valid CAS Registry Number.

53859-25-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name methyl 2-(6-chloro-1H-indol-3-yl)acetate

1.2 Other means of identification

Product number -
Other names Methyl-6-chlorindolyl-3-acetat

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:53859-25-9 SDS

53859-25-9Relevant academic research and scientific papers

Organocatalyzed enantioselective fluorocyclizations

Lozano, Oscar,Blessley, George,Martinez Del Campo, Teresa,Thompson, Amber L.,Giuffredi, Guy T.,Bettati, Michela,Walker, Matthew,Borman, Richard,Gouverneur, Veronique

, p. 8105 - 8109 (2011/10/03)

Enantioenriched fluorinated heterocycles can be prepared through fluorocyclizations of prochiral indoles (see scheme; Ts=tosyl, Bn=benzyl, Boc=tert-butoxycarbonyl). More than twenty examples for this cascade fluorination-cyclization, which is catalyzed by cinchona alkaloids and employs N-fluorobenzenesulfonimide as the electrophilic fluorine source have been explored, and an unprecedented catalytic asymmetric difluorocyclization has also been identified.

INDOLECARBOXYLIC ACID DERIVATIVE HAVING PGD2 RECEPTOR ANTAGONISTIC ACTIVITY

-

Page/Page column 65, (2008/06/13)

Indolecarboxylic acid derivatives having DP receptor antagonistic activity and pharmaceutical compositions containing the compounds as active ingredients; and further relevant therapeutic agents for allergic diseases. There are provided compounds, their pharmaceutically acceptable salts or solvates thereof, the compounds represented by the general formula: (I) wherein the ring A is an aromatic carbon ring, etc.; the ring B is a nonaromatic-nitrogen-containing heterocycle, etc.; the formula -X1=X2-X3=X4- is the formula -C(R1)=C(R2)-C(R3)=C(R4)-, etc.; X5 is C(R5) or N; each of R1, R2, R3, R4 and R5 independently is a hydrogen atom, a halogen atom, etc.; R6 is the formula -Z-R10 (in which Z is alkylene, etc.; and R10 is carboxyl, etc.), etc.; R7 is an optionally substituted alkyloxy, etc.; each of R8s independently is a halogen atom, etc.; each of R9s independently is an optionally substituted alkyl, etc.; Y is a single bond, etc.; n is 0, etc.; and q is 0, etc.

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