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6623-99-0

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6623-99-0 Usage

Type of compound

Chemical compound

Use

Fungicide to control various plant diseases

Mechanism of action

Inhibits succinate dehydrogenase enzyme in the respiratory chain of fungi, disrupting their energy production and leading to their death

Effectiveness

Effective against a wide range of plant pathogenic fungi

Benefits

Valuable tool for farmers and gardeners to protect crops from diseases

Toxicity

Low toxicity to mammals and non-target organisms

Approval

Approved for use in various countries for agricultural purposes

Check Digit Verification of cas no

The CAS Registry Mumber 6623-99-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,6,2 and 3 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 6623-99:
(6*6)+(5*6)+(4*2)+(3*3)+(2*9)+(1*9)=110
110 % 10 = 0
So 6623-99-0 is a valid CAS Registry Number.

6623-99-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(2-methylpropanoyl)isoindole-1,3-dione

1.2 Other means of identification

Product number -
Other names N-Isobutyryl-phthalimid

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:6623-99-0 SDS

6623-99-0Downstream Products

6623-99-0Relevant articles and documents

GONADOTROPIN-RELEASING HORMONE RECEPTOR ANTAGONISTS AND METHODS RELATING THERETO

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Page 29, (2010/02/10)

GnRH receptor antagonists are disclosed that have utility in the treatment of a variety of sex-hormone related conditions in both men and women. The compounds of this invention have the structure: wherein n, R1a, R1b, R1c, R2a, R2b, R3, R4, R5, R6 and X are as defined herein, including stereoisomers, prodrugs and pharmaceutically acceptable salts thereof. Also disclosed are compositions containing a compound of this invention in combination with a pharmaceutically acceptable carrier, as well as methods relating to the use thereof for antagonizing gonadotropin-releasing hormone in a subject in need thereof.

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