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2-chloro-l-decyl

The rrans-diacetoxycyclohexane was almost the sole product when the refluxing mixture contained tellurium dioxide and lithium bromide3. 2-Chloro-l-decyl tellurium trichloride in refluxing acetic acid in the presence of tellurium dioxide and lithium bromide formed 1,2-diacetoxydecane3. [Pg.335]

H17C9 H CHCla/benzoqiiinone threo-l-D-2-chloro-l-decyl >97 oil 2... [Pg.302]

Telluran(IV) (2-Chloro-l-deutero-decyl)-trichloro- E21e, 5127 (En + TeCl4)... [Pg.813]

Chloro-l-Hydroxybenzene 25167-80-0 cis-9-Octadecenoic Acid 112-80-1 Decyl Alcohol 112-30-1... [Pg.3474]

In a similar way, numerous P-chloroalkylphosphonic acids undergo fast and quantitative hydrolysis at pH > 5 94). A typical example is the fragmentation of 2-chloro-decyl-l-phosphonic acid in the presence of cyclohexylamine with formation of 1-decene (in contrast, other bases such as pyridine, triethylamine, and dimethylaniline effect only HC1 elimination to form 1-decene-l-phosphonic acid). Added alcohols, such as ethanol, allyl alcohol, cyclohexanol, tert-butanol, and phenol are phosphorylat-ed. [Pg.104]

D<>decyl-2-hydroxy-5-methylphenyl)(2-hydroxyphenyl)methanone, 440 Bis[5-chloro-3-(5-chloro-2-hydroxybenzoyl)-2-hydroxyphenyl]methanone, 540 Bis[5-fluoro-3-(5-fluoro-2-hydroxybenzoyl)-2-hydroxyphenyl]methanone, 540 (2,4-Dihydroxy-l,3,5-benzenetriyl)tris[phenylmethanone, 540... [Pg.2475]


See other pages where 2-chloro-l-decyl is mentioned: [Pg.302]    [Pg.302]    [Pg.302]    [Pg.302]    [Pg.302]    [Pg.302]    [Pg.302]    [Pg.302]    [Pg.302]   
See also in sourсe #XX -- [ Pg.302 ]

See also in sourсe #XX -- [ Pg.302 ]




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