52323-99-6

Basic information

• Product Name: 1-broMo-4,4-diMethyl-2-pentyne
• Synonyms: 1-broMo-4,4-diMethyl-2-pentyne
• CAS NO: 52323-99-6
• Molecular Formula: C₇H₁₁Br
• Molecular Weight: 175.06624
• Mol File: 52323-99-6.mol
• Article Data: 7

Chemical Properties

• Boiling Point: 164.7±23.0 °C(Predicted)
• Appearance: /
• Density: 1.245±0.06 g/cm3(Predicted)
• CAS DataBase Reference: 1-broMo-4,4-diMethyl-2-pentyne(CAS DataBase Reference)
• NIST Chemistry Reference: 1-broMo-4,4-diMethyl-2-pentyne(52323-99-6)
• EPA Substance Registry System: 1-broMo-4,4-diMethyl-2-pentyne(52323-99-6)

Safety Data

• Hazardous Substances Data: 52323-99-6(Hazardous Substances Data)

Usage

Physical state

Colorless liquid at room temperature

Family

Alkynes

Functional group

Alkyl bromide

Carbon-carbon triple bond

Present

Bromine atom

Attached to the carbon chain

Industrial and laboratory applications

Widely used

Importance

Significant in the field of organic chemistry

Upstream product

• 52323-98-5 4,4-dimethylpent-2-yn-1-ol 
• 917-92-0 3,3-Dimethylbut-1-yne 
• 104480-60-6 (3,3-dimethylbut-1-yn-1-yl)magnesium bromide 

Downstream Products

• 72040-26-7 1-(4,4-dimethyl-pent-2-ynyl)-2-phenyl-1H-arsinin-4-one 
• 124156-14-5 1-(4,4-dimethyl-2-pentynyl)cyclohexanol 
• 124156-18-9 5,5-dimethyl-1-phenyl-3-hexyn-1-ol 
• 88096-95-1 (4,4-dimethylpent-2-ynylsulfanyl)benzene 
• 88096-96-2 4,4-dimethyl-1-phenylthio-1,2-pentadiene 
• 113439-90-0 4,4-dimethylpent-2-yn-1-amine 
• 61652-71-9 4,4-dimethyl-3-oxo- N-phenylpentanamide 

Relevant articles and documents

Catalytic asymmetric synthesis of substituted morpholines and piperazines

Under two conditions: Hydroamination catalyzed by group 4 metals is featured in the modular and enantioselective synthesis of 3-substituted morpholines and the diastereoselective synthesis of 2,5-substituted piperazines. Copyright

Substituted 4-aminocyclohexane derivatives

Substituted 4-aminocyclohexane derivatives having the formula I: [image] wherein R1-R4 are as described herein, methods for their preparation, medicinal products and pharmaceutical compositions containing these compounds and the use of substituted 4-amino

A direct route to conjugated enediynes from dipropargylic sulfones by a modified one-flask Ramberg-Baecklund reaction

The reaction of dipropargylic sulfones with dibromodifluoromethane in the presence of alumina-supported KOH in dichloromethane solution results in facile rearrangement affording the corresponding conjugated linear and cyclic enediynes in good yields. This result shows that the direct transformation of a- and a′-hydrogen bearing sulfones assembles enediyne units without resorting to the prior preparation of the a-halo sulfone precursors in a separate step.