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Citronellyl acetate
- Name Citronellyl acetate
- CAS 150-84-5
- Purity 99%
Product Details
Chemical plants supply high-quality Citronellyl acetate 150-84-5 in bulk
- Molecular Formula: C12H22O2
- Molecular Weight: 198.305
- Appearance/Colour: clear colorless liquid
- Vapor Pressure: 1.97Pa at 20℃
- Melting Point: 17.88°C (estimate)
- Refractive Index: n20/D 1.445(lit.)
- Boiling Point: 258.5 °C at 760 mmHg
- Flash Point: 88.2 °C
- PSA： 26.30000
- Density: 0.885 g/cm3
- LogP: 3.32210
150-84-5 Relevant articles
Sn(II)-catalyzed β-citronellol esterification: A Bronsted acid-free process for synthesis of fragrances at room temperature
Da Silva,Julio,Dos Santos
, p. 1261 - 1266 (2015)
Simple SnCl2·2H2O was demonstrated to be...
Solid state acetylation with acetylimidazole: Selective protection of primary alcohols and phenols
Hagiwara, Hisahiro,Morohashi, Kimie,Suzuki, Toshio,Ando, Masayoshi,Yamamoto, Isao,Kato, Michiharu
, p. 2001 - 2006 (1998)
Primary alcohols and phenols have been a...
Synthesis of citronellyl acetate via a transacetylation to citronellol from acetyl coenzyme A produced from glucose and acetate in growing yeasts
Oda, Shinobu,Sugai, Takeshi,Ohta, Hiromichi
, p. 500 - 501 (2001)
A novel coupling system, which is an ace...
LUMINALLY-ACTING N-(PIPERIDIN-4-YL)BENZAMIDE DERIVATIVES
-
Paragraph 0219; 0220, (2021/11/13)
Disclosed are compounds of Formula 1, an...
Ring-Closing Metathesis of Aliphatic Ethers and Esterification of Terpene Alcohols Catalyzed by Functionalized Biochar
Kerton, Francesca M.,MacQuarrie, Stephanie L.,Vidal, Juliana L.,Wyper, Olivia M.
supporting information, p. 6052 - 6056 (2021/12/10)
Functionalized biochars, renewable carbo...
Method for synthesizing acetate perfume
-
Paragraph 0063-0066, (2021/01/15)
The invention provides a method for synt...
IrIII-Catalyzed direct syntheses of amides and esters using nitriles as acid equivalents: A photochemical pathway
Talukdar, Ranadeep
supporting information, p. 5303 - 5308 (2020/04/17)
An unprecedented IrIII[df(CF3)ppy]2(dtbb...
150-84-5 Process route
-
-
(6-acetoxy-1-isopropenyl-4-methylhexyl)dimethylsulfonium perchlorate
-
-
150-84-5,67650-82-2
citronellyl-acetate
-
-
141-11-7
3,7-dimethyl-7-octen-1-ol acetate
-
-
161013-76-9
3,7-Dimethyl-6-methylthiooct-7-en-1-ol acetate
| Conditions | Yield |
|---|---|
|
With
lithium perchlorate;
In
N,N-dimethyl-formamide;
Yields of byproduct given;
E = -1.7 V;
|
15%
|
-
-
(6-acetoxy-1-isopropenyl-4-methylhexyl)dimethylsulfonium perchlorate
-
-
150-84-5,67650-82-2
citronellyl-acetate
-
-
141-11-7
3,7-dimethyl-7-octen-1-ol acetate
-
-
3,7,10,14-tetramethylhexadeca-6,10-diene-1,16-diol diacetate
| Conditions | Yield |
|---|---|
|
With
lithium perchlorate;
In
N,N-dimethyl-formamide;
Yields of byproduct given;
E = -1.25 V;
|
10%
|
|
With
lithium perchlorate;
In
N,N-dimethyl-formamide;
Product distribution;
Mechanism;
various electrode potentials;
|
150-84-5 Upstream products
-
106-22-9
Citronellol
-
109143-32-0
8-acetoxy-2,6-dimethyl-3-methylseleno-2-hydroxyoctane
-
108-24-7
acetic anhydride
-
2466-76-4
N-Acetylimidazole
150-84-5 Downstream products
-
64309-03-1
6-isopropenyl-3-methyl-9-decenyl acetate
-
67601-01-8
1-Benzenesulfonyl-10-hydroxy-5-isopropenyl-8-methyl-decan-2-one
-
67601-02-9
10-Benzenesulfonyl-6-isopropenyl-3-methyl-decane-1,9-diol
-
5523-95-5
3,7-dimethyloctyl acetate
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