CAS 13280-07-4

4-Chloro-2-butyn-1-ol

Description:

4-Chloro-2-butyn-1-ol is an organic compound characterized by its alkyne functional group and the presence of a hydroxyl group. It features a four-carbon chain with a chlorine atom attached to the fourth carbon and a triple bond between the second and third carbons. This compound is typically a colorless to pale yellow liquid and is known for its reactivity due to the presence of both the alkyne and alcohol functional groups. It is soluble in organic solvents and exhibits moderate polarity due to the hydroxyl group. 4-Chloro-2-butyn-1-ol can participate in various chemical reactions, including nucleophilic substitutions and eliminations, making it useful in organic synthesis. Safety precautions are necessary when handling this compound, as it may be toxic and irritant. Its applications may extend to pharmaceuticals, agrochemicals, and as an intermediate in organic synthesis. Proper storage and handling in a well-ventilated area are recommended to mitigate any health risks associated with exposure.

Formula: C₄H₅ClO

InChI: InChI=1/C4H5ClO/c5-3-1-2-4-6/h6H,3-4H2

InChI key: InChIKey=RPUJAOFSZSEVPC-UHFFFAOYSA-N

SMILES: C(#CCO)CCl

Synonyms:

• 1-Chloro-2-butyn-4-ol
• 1-Chloro-4-hydroxy-2-butyne
• 2-Butyn-1-ol, 4-chloro-
• 4-Chloro-2-butyne-1-ol
• 4-Chloro-2-butynol
• 4-Chlorobut-2-Yn-1-Ol
• Brn 1098382
• 4-01-00-02220 (Beilstein Handbook Reference)
• 4-Chloro-2-butyn-1-ol
• 4-chloro-2-butyn-1-o
• 4-chloro-2-butan-1-ol
• LIGAMO-001

2-Butyn-1-ol, 4-chloro-

CAS: 13280-07-4

Formula: C₄H₅ClO

Purity: 95%

Color and Shape: Liquid

Molecular weight: 104.5349

Ref: IN-DA00117F

4-Chlorobut-2-yn-1-ol

CAS: 13280-07-4

4-Chlorobut-2-yn-1-ol

Purity: 98%

Molecular weight: 104.53g/mol

Ref: 54-OR91532

4-Chlorobut-2-yn-1-ol

CAS: 13280-07-4

Purity: 95%

Color and Shape: Liquid

Molecular weight: 104.5299988

Ref: 10-F674135

4-Chloro-2-butyn-1-ol

CAS: 13280-07-4

4-Chloro-2-butyn-1-ol is an allylic alcohol that has been used in the synthesis of nitroalkenes. The diastereoselective synthesis of 4-chloro-2-butyn-1-ol can be achieved by the reaction of nitroalkenes with copper(II) salts, which are trackable and extracted. The cross coupling reaction can also be used to produce this compound. The reactivity and mediation of 4-chloro-2-butyn-1-ol can be attributed to its diastereoselective nature. Gamma linolenic acid is a fatty acid that contains four double bonds in a row on the same side of the molecule, and it is found in plant sources such as hemp oil. Copper sulfinates are known for their diastereoselectivity in their synthesis, which may account for the high yields of 4-chloro 2 butyn 1 ol obtained from these compounds.

Formula: C₄H₅ClO

Purity: Min. 95 Area-%

Color and Shape: Clear Liquid

Molecular weight: 104.53 g/mol

Ref: 3D-FC161946