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114305-99-6

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114305-99-6 Usage

General Description

6-CHLORO-3-INDOLYL ACETATE is a chemical compound with the molecular formula C10H8ClNO2. It is a derivative of indole and is commonly used as a substrate in the detection and quantification of indole-3-acetic acid, a plant hormone that plays a crucial role in regulating plant growth and development. 6-CHLORO-3-INDOLYL ACETATE is often used in biochemical research and is also employed in the analysis of hormone levels in plant tissues. Its structural similarity to indole-3-acetic acid allows for specific and sensitive detection methods, making it a valuable tool for studying plant physiology and biochemistry.

Check Digit Verification of cas no

The CAS Registry Mumber 114305-99-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,4,3,0 and 5 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 114305-99:
(8*1)+(7*1)+(6*4)+(5*3)+(4*0)+(3*5)+(2*9)+(1*9)=96
96 % 10 = 6
So 114305-99-6 is a valid CAS Registry Number.

114305-99-6SDS

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 (6-chloro-1H-indol-3-yl) acetate

1.2 Other means of identification

Product number -
Other names BIC1358

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:114305-99-6 SDS

114305-99-6Downstream Products

114305-99-6Relevant articles and documents

THIOINDIRUBINS

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Paragraph 0407; 0410-0412; 0413, (2019/03/17)

Disclosed herein inter alia are compositions and methods for treating cancer using thioindirubin derivatives.

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