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2,2,3-Trichlorobutyraldehyde is a chemical compound characterized by its molecular formula C4H4Cl3O. It is an aldehyde, which means it contains a carbonyl group (C=O) bonded to at least one hydrogen atom. This colorless to pale yellow liquid exhibits a pungent odor and is recognized for its reactivity as an intermediate in the synthesis of various organic compounds. Its chemical properties and potential health hazards necessitate careful handling and storage in industrial and laboratory environments.

76-36-8

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76-36-8 Usage

Uses

Used in Pharmaceutical Industry:
2,2,3-Trichlorobutyraldehyde is used as a key intermediate in the synthesis of pharmaceuticals for its ability to readily participate in chemical reactions, contributing to the development of new drugs and medicinal compounds.
Used in Agrochemical Industry:
In the agrochemical sector, 2,2,3-trichlorobutyraldehyde serves as an essential intermediate, facilitating the production of various agrochemicals that are vital for crop protection and enhancement of agricultural yields.
Used in Organic Compounds Synthesis:
2,2,3-Trichlorobutyraldehyde is utilized as a reactive intermediate in the synthesis of a wide range of organic compounds, showcasing its versatility in organic chemistry and its importance in creating new chemical entities for various applications.

Check Digit Verification of cas no

The CAS Registry Mumber 76-36-8 includes 5 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 2 digits, 7 and 6 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 76-36:
(4*7)+(3*6)+(2*3)+(1*6)=58
58 % 10 = 8
So 76-36-8 is a valid CAS Registry Number.

76-36-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,2,3-trichlorobutanal

1.2 Other means of identification

Product number -
Other names Butyraldehyde,2,2,3-trichloro

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:76-36-8 SDS

76-36-8Relevant academic research and scientific papers

Synthesis and reactivity of novel α,α,β- and α,α,δ-trichlorinated imines

D'Hooghe, Matthias,De Meulenaer, Bruno,De Kimpe, Norbert

scheme or table, p. 2437 - 2442 (2009/04/08)

A variety of different N-(2,2,3-trichloropropylidene)amines, N-(2,2,3-trichlorobutylidene)amines, and N-(2,2,5-trichloropentylidene)amines were synthesized for the first time, and their reactivity with regard to hydride reagents was investigated. In this way, N-(2,2,5-trichloropentylidene)amines were evaluated as substrates for the synthesis of piperidines, and N-(2,2,3-trichloropropylidene)amines and N-(2,2,3-trichlorobutylidene)amines were reduced efficiently into the corresponding novel β,β,γ- trichloroamines by means of sodium cyanoborohydride in methanol in the presence of acetic acid. Furthermore, N-(2,2,3-trichloropropylidene)amines were transformed into 2-(chloromethyl)aziridines by lithium aluminium hydride in Et2O, and N-(2,2,5-trichloropentylidene)acetamide was used for the first time as a suitable substrate for the addition of oxygen, nitrogen, and sulfur nucleophiles in good yields. Georg Thieme Verlag Stuttgart.

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