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2-(tert-butylamino)-1-(4,5-dichlorothiophen-2-yl)ethanol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

38450-46-3

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38450-46-3 Usage

Chemical class

Triazines (a type of herbicide)

Function

Selective herbicide that inhibits photosynthesis and other essential plant processes

Usage

Controlling weeds in various crops like corn, soybeans, and sugarcane

Mammalian toxicity

Low toxicity to mammals

Bioaccumulation

Not expected to bioaccumulate in the environment

Environmental concerns

Groundwater contamination and potential harm to non-target organisms

Safety and environmental regulations

Usage and handling should comply with strict safety and environmental regulations

Check Digit Verification of cas no

The CAS Registry Mumber 38450-46-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,8,4,5 and 0 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 38450-46:
(7*3)+(6*8)+(5*4)+(4*5)+(3*0)+(2*4)+(1*6)=123
123 % 10 = 3
So 38450-46-3 is a valid CAS Registry Number.

38450-46-3SDS

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 2-(tert-butylamino)-1-(4,5-dichlorothiophen-2-yl)ethanol

1.2 Other means of identification

Product number -
Other names QM-5119

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:38450-46-3 SDS

38450-46-3Downstream Products

38450-46-3Relevant academic research and scientific papers

Bromothiophene Reactions. II. A Novel Rearrangement in the Zinc and Acetic Acid Reduction

Alvares-Insua, A. S.,Conde, S.,Corral, C.

, p. 713 - 716 (2007/10/02)

The elimination of the α-bromine atoms of the bromothienylethanolamine derivatives 2a, b, c, d with zinc and acetic acid unexpectedly involved a migration of the ethanolamine side chain from the 3 to the 2 position in the thiophene ring.Experiments carried out with simpler analogous compounds 3, 4 and 6 seem to indicate that this rearrangement takes place only in those cases in which the carbon atom of the side chain next to the ring supports an oxygen atom capable of being protonated in the reaction medium.A tentative mechanism is proposed to explain the experimental results.

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