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2-(3,5-Dichlorophenoxy)-2-Methylpropanoic acid is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

33995-37-8

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33995-37-8 Usage

Classification

Synthetic auxin herbicide

Function

Controls broadleaf weeds in agriculture

Mechanism

Disrupts plant growth and causes uncontrolled cell division, leading to plant death

Environmental persistence

Can persist in soil, water, and air

Environmental and health concerns

Drift damage to non-target crops, water contamination, potential human health risks

Use in agriculture

Commonly used, particularly in genetically modified crops that are resistant to its effects.

Check Digit Verification of cas no

The CAS Registry Mumber 33995-37-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,3,9,9 and 5 respectively; the second part has 2 digits, 3 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 33995-37:
(7*3)+(6*3)+(5*9)+(4*9)+(3*5)+(2*3)+(1*7)=148
148 % 10 = 8
So 33995-37-8 is a valid CAS Registry Number.

33995-37-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(3,5-Dichlorophenoxy)-2-methylpropanoic acid

1.2 Other means of identification

Product number -
Other names -

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:33995-37-8 SDS

33995-37-8Downstream Products

33995-37-8Relevant academic research and scientific papers

Exploration of a 14-3-3 PPI Pocket by Covalent Fragments as Stabilizers

Sijbesma, Eline,Hallenbeck, Kenneth K.,Andrei, Sebastian A.,Rust, Reanne R.,Adriaans, Joris M. C.,Brunsveld, Luc,Arkin, Michelle R.,Ottmann, Christian

, p. 976 - 982 (2021/05/27)

The systematic discovery of functional fragments binding to the composite interface of protein complexes is a first critical step for the development of orthosteric stabilizers of protein-protein interactions (PPIs). We have previously shown that disulfide trapping successfully yielded covalent stabilizers for the PPI of 14-3-3 with the estrogen receptor ERα. Here we provide an assessment of the composite PPI target pocket and the molecular characteristics of various fragments binding to a specific subpocket. Evaluating structure-activity relationships highlights the basic principles for PPI stabilization by these covalent fragments that engage a relatively large and exposed binding pocket at the protein/peptide interface with a "molecular glue"mode of action.

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