994-25-2

Basic information

• Product Name: 3-chloro-3-ethylpentane
• Synonyms: 3-Chloro-3-ethylpentane; pentane, 3-chloro-3-ethyl-
• CAS NO: 994-25-2
• Molecular Formula: C₇H₁₅Cl
• Molecular Weight: 134.647
• Mol File: 994-25-2.mol
• Article Data: 4

Chemical Properties

• Boiling Point: 143.5°C at 760 mmHg
• Flash Point: 33.5°C
• Density: 0.865g/cm³
• Vapor Pressure: 6.68mmHg at 25°C
• Refractive Index: 1.419
• CAS DataBase Reference: 3-chloro-3-ethylpentane(CAS DataBase Reference)
• NIST Chemistry Reference: 3-chloro-3-ethylpentane(994-25-2)
• EPA Substance Registry System: 3-chloro-3-ethylpentane(994-25-2)

Safety Data

• Hazardous Substances Data: 994-25-2(Hazardous Substances Data)

Upstream product

• 597-49-9 3-ethylpentan-3-ol 
• 816-79-5 3-ethyl-2-pentene 
• 35354-15-5 2,2-diethylbutanoyl chloride 
• 7647-01-0 hydrogenchloride 
• 64-19-7 acetic acid 
• 96-22-0 pentan-3-one 
• 7446-70-0 aluminium trichloride 
• 71-43-2 benzene 

Downstream Products

• 816-79-5 3-ethyl-2-pentene 
• 4170-84-7 (1,1-diethyl-propyl)-benzene 
• 4468-40-0 (1-ethyl-1-methyl-butyl)-benzene 
• 5171-86-8 3,3,4,4-tetraethyl-hexane 
• 1067-08-9 3-ethyl-3-methyl-pentane 
• 69719-09-1 (1,1,2-trimethyl-butyl)-benzene 
• 92860-85-0 3-(1,1-Diethylpropyl)-cyclohex-4-en-1,2-dicarbonsaeure 

Relevant articles and documents

Direct halogenation of alcohols with halosilanes under catalyst- and organic solvent-free reaction conditions

A chemoselective method for the direct halogenation of different types of alcohols with halosilanes under catalyst- and solvent-free reaction conditions (SFRC) is reported. Various primary, secondary and tertiary benzyl alcohols and tertiary alkyl alcohols were directly transformed to the corresponding benzyl and alkyl halides, respectively, using chlorotrimethylsilane (TMSCl) and bromotrimethylsilane (TMSBr).

Steroidal Silicon Side-Chain Analogues as Potential Antifertility Agents

A number of silicon-substituted analogues of ethynylestradiol that exhibit modified and enhanced biological activities have been synthesized.Particularly noteworthy are a group of estradiol analogues that exhibit high antifertility potency and markedly reduced estrogenic activity.The best compounds synthesized are 17α-estradiol (5) and 17α-estradiol (33), which show a separation of antifertility from estrogenic activity in the rat.The results of structure-activity studies indicate a good correlation between the observed biological activities and the calculated van der Waals volumes of the three variable silicon substituents.