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Butanoic acid, 4-[[(1,1-dimethylethoxy)carbonyl]amino]-3-oxo-, 1,1-dimethylethyl ester, commonly known as DEET, is a synthetic chemical compound widely recognized as an effective insect repellent. It functions by obstructing insects' ability to detect the carbon dioxide and lactic acid emitted by humans, thereby repelling mosquitoes, ticks, and other biting insects. DEET is typically applied to the skin, clothing, or other surfaces to offer long-lasting protection against insect bites. However, it is crucial to use DEET in moderation and adhere to the recommended usage guidelines to minimize potential health risks associated with overexposure.

144572-32-7

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144572-32-7 Usage

Uses

Used in Personal Protection:
Butanoic acid, 4-[[(1,1-dimethylethoxy)carbonyl]amino]-3-oxo-, 1,1-dimethylethyl ester is used as an insect repellent for personal protection against mosquito bites, ticks, and other biting insects. It provides long-lasting protection when applied to the skin or clothing, helping to reduce the risk of insect-borne diseases.
Used in Outdoor Activities:
In the Outdoor and Recreational Activities industry, Butanoic acid, 4-[[(1,1-dimethylethoxy)carbonyl]amino]-3-oxo-, 1,1-dimethylethyl ester is used as an insect repellent to ensure safety and comfort during outdoor adventures. It helps protect individuals from insect bites, allowing them to enjoy their activities without the worry of insect-borne diseases.
Used in Military and Field Operations:
In the Military and Field Operations industry, Butanoic acid, 4-[[(1,1-dimethylethoxy)carbonyl]amino]-3-oxo-, 1,1-dimethylethyl ester is used as an insect repellent to safeguard soldiers and personnel from insect-borne diseases during field operations. It is applied to uniforms and equipment to provide protection against mosquitoes, ticks, and other biting insects in various environments.
Used in Public Health and Disease Prevention:
In the Public Health and Disease Prevention industry, Butanoic acid, 4-[[(1,1-dimethylethoxy)carbonyl]amino]-3-oxo-, 1,1-dimethylethyl ester is used as an insect repellent to reduce the transmission of insect-borne diseases such as malaria, dengue fever, and Lyme disease. It is an essential tool in vector control programs and helps protect communities from these potentially life-threatening diseases.

Check Digit Verification of cas no

The CAS Registry Mumber 144572-32-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,4,5,7 and 2 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 144572-32:
(8*1)+(7*4)+(6*4)+(5*5)+(4*7)+(3*2)+(2*3)+(1*2)=127
127 % 10 = 7
So 144572-32-7 is a valid CAS Registry Number.

144572-32-7SDS

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 tert-butyl <(tert-butoxycarbonyl)amino>-3-oxo-butanoate

1.2 Other means of identification

Product number -
Other names 4-tert-Butoxycarbonylamino-3-oxo-butyric 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:144572-32-7 SDS

144572-32-7Downstream Products

144572-32-7Relevant academic research and scientific papers

Synthesis of (2RS,E)-3-Ethylidene-azetidine-2-carboxylic acid (rac. polyoximic acid)

Emmer, Gerhard

, p. 7165 - 7172 (2007/10/02)

Treatment of α-diazo β-ketoester 4 with a catalytic amount of rhodium (II) acetate followed by Wittig reaction with phosphorane 5 gave the isomeric phenylthioester derivative 6a and 6b. Reduction of 6a led to the corresponding allylic alcohol 7, which was further converted into the bromide 8. Dehalogenation of 8 with NaBH4/ DMF resulted in compound 9, which was deprotected with trifluoroacetic acid, giving racemic polyoximic acid (1).

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