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alicyclic
alicyclic, a. Chem. (ælɪˈsɪklɪk, -ˈsaɪk-) [ad. G. alicyclisch (E. Bamberger 1889, in Ber. d. Deut. Chem. Ges. XXII. 767), f. aliphatic a. + cyclic a. 7.] Combining the properties of aliphatic and cyclic compounds (see cyclic a. 7).1891 Jrnl. Chem. Soc. LX. ii. 1097 Alicyclic Homology. 1900 E. F. Smi...
Oxford English Dictionary
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Alicyclic compound
Alicyclic compounds may have one or more aliphatic side chains attached. The mode of ring-closing in the formation of many alicyclic compounds can be predicted by Baldwin's rules.
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Alicycliphilus
fat-like organic compounds; Neo-Latin adjective from Greek adjective () meaning friend, loving; Neo-Latin masculine gender adjective Alicycliphilus, alicyclic
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-oic
-oic ending of the names of organic acids containing a carboxyl group, esp. in place of a methyl group. [App. first used in caproic a.]1971 Nomencl. Org. Chem. (I.U.P.A.C.) (ed. 2) C. 182 Carboxyl groups COOH replacing CH3 at the end of the main chain of an alicyclic hydrocarbon are denoted by addin...
Oxford English Dictionary
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Cyclononane
Cyclononane is an alicyclic hydrocarbon consisting of a ring of nine carbon atoms. Its molecular formula is C9H18.
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Cyclopentamine
The effect that this has on potency is that the reduced alicyclic-alkylamines are weaker than unsaturated (meth)amphetamine.
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4-Methylcyclohexanemethanol
Classified as a saturated higher alicyclic primary alcohol. General chemical class and closely related compounds
A World Health Organization study of the toxicity of alicyclic primary alcohols and related alicyclic
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Preparation of alicyclic carboxylic acids - Google Patents
B01J23/00 — Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00
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Malonic ester synthesis
This reaction is also called the Perkin alicyclic synthesis (see: alicyclic compound) after investigator William Henry Perkin, Jr.
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丙二酸酯合成
参见
克诺维纳盖尔缩合(Knoevenagel condensation)
(Perkin alicyclic synthesis)
乙醯乙酸酯合成
参考资料
取代反应
碳-碳键形成反应
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Cypenamine
Homology
Cypenamine is a homolog of tranylcypromine, containing an expanded alicyclic ring that is two methylene units larger than the highly strained/
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Hydroxylamine-O-sulfonic acid
It is used as a reagent for the introduction of amine groups (–NH2), for the conversion of aldehydes into nitriles and alicyclic ketones into lactams ( When heated to reflux for several hours under acidic conditions (e.g., in the presence of concentrated formic acid) alicyclic ketones react to provide
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CGS-20625
Due to its alicyclic moiety potency at γ1 subunit, containing receptor types is more pronounced for CGS-20625 compared to benzodiazepines. γ1 subunits
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Synthetic musk
musks
Alicyclic musks, otherwise known as cycloalkyl ester or linear musks, are a relatively novel class of musk compounds. Romandolide, a more ambrette and less fruity alicyclic musk compared to Helvetolide, was introduced ten years later.
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Otto Wallach
Otto Wallach (; 27 March 1847 – 26 February 1931) was a German chemist and recipient of the 1910 Nobel Prize in Chemistry for his work on alicyclic compounds See also
List of Jewish Nobel laureates
References
External links
including the Nobel Lecture, December 12, 1910 Alicyclic Compounds
1847 births
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