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185063-82-5

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185063-82-5 Usage

Description

(4-Hydroxy-5-isopropyl-2-methyl-phenyl)-carbamic acid tert-butyl ester, also known as tiocarbazil, is a synthetic chemical compound with potent fungicidal properties. It is characterized by its ability to inhibit fungal growth by disrupting cell structure and interfering with fungal metabolism, making it a valuable asset in agricultural practices.
Used in Agricultural Industry:
(4-Hydroxy-5-isopropyl-2-methyl-phenyl)-carbamic acid tert-butyl ester is used as a fungicide for controlling a broad spectrum of plant diseases. It is effective against common afflictions such as powdery mildew, leaf spot, and rust, thereby protecting crops and ensuring a healthy yield.

Check Digit Verification of cas no

The CAS Registry Mumber 185063-82-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,8,5,0,6 and 3 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 185063-82:
(8*1)+(7*8)+(6*5)+(5*0)+(4*6)+(3*3)+(2*8)+(1*2)=145
145 % 10 = 5
So 185063-82-5 is a valid CAS Registry Number.

185063-82-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name tert-butyl N-(4-hydroxy-2-methyl-5-propan-2-ylphenyl)carbamate

1.2 Other means of identification

Product number -
Other names (4-Hydroxy-5-isopropyl-2-methyl-phenyl)-carbamic acid tert-butyl ester

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:185063-82-5 SDS

185063-82-5Relevant articles and documents

Indole inhibitors of human nonpancreatic secretory phospholipase A2. 1. Indole-3-acetamides

Dillard, Robert D.,Bach, Nicholas J.,Draheim, Susan E.,Berry, Dennis R.,Carlson, Donald G.,Chirgadze, Nickolay Y.,Clawson, David K.,Hartley, Lawrence W.,Johnson, Lea M.,Jones, Noel D.,McKinney, Emma R.,Mihelich, Edward D.,Olkowski, Jennifer L.,Schevitz, Richard W.,Smith, Amy C.,Snyder, David W.,Sommers, Cynthia D.,Wery, Jean-Pierre

, p. 5119 - 5136 (2007/10/03)

Phospholipases (PLAs) produce rate-limiting precursors in the biosynthesis of various types of biologically active lipids involved in inflammatory processes. Increased levels of human nonpancreatic secretory phospholipase A2 (hnps-PLA2) have been detected in several pathological conditions. An inhibitor of this enzyme could have therapeutic utility. A broad screening program was carried out to identify chemical structures which could inhibit hnps-PLA2. One of the lead compounds generated by the screening program was 5-methoxy-2-methyl-1-(phenylmethyl)-1H-indole-3-acetic acid (13a). We describe the syntheses, structure-activity relationships, and pharmacological activities of a series of indole-3-acetamides and related compounds derived from this lead. This SAR was undertaken with the aid of X- ray crystal structures of complexes between the inhibitors and hnps-PLA2 which were of great value in directing the SAR.

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