Purity 99% Min 2-SEC-BUTYLCYCLOHEXANONE 14765-30-1 Spot Supply with Safe Transportation
- Molecular Formula: C10H18 O
- Molecular Weight: 154.252
- Vapor Pressure: 0.163mmHg at 25°C
- Melting Point: 27.18°C (estimate)
- Refractive Index: n20/D 1.458(lit.)
- Boiling Point: 76-78 °C8 mm Hg(lit.)
- Flash Point: 181 °F
- PSA： 17.07000
- Density: 0.912 g/mL at 25 °C(lit.)
- LogP: 2.79180
2-SEC-BUTYLCYCLOHEXANONE(Cas 14765-30-1) Usage
|
Preparation |
By hydrogenation of o-sec-butyl phenol in the presence of palladium catalyst; by hydrogenation of 2-sec-butylidene cyclohexanone. |
|
Aroma threshold values |
Aroma characteristics at around 1.0%: cooling minty, menthol-like, spearmint green, slightly spicy, woody with a vapor action note. |
|
Taste threshold values |
Taste characteristics at 20 ppm: minty, cooling, candy cane peppermint with a slight green nuance. |
|
Flammability and Explosibility |
Notclassified |
InChI:InChI=1/C10H18O/c1-3-8(2)9-6-4-5-7-10(9)11/h8-9H,3-7H2,1-2H3
14765-30-1 Relevant articles
1,4-Addition of diorganozincs to α,β-unsaturated ketones catalyzed by a copper(I)-sulfonamide combined system
Kitamura, Masato,Miki, Takashi,Nakano, Keiji,Noyori, Ryoji
, p. 999 - 1014 (2000)
A mixture of CuCN and N-benzylbenzenesul...
Serine carbonates
-
, (2008/06/13)
Serine carbonates of formula I are precu...
Compounds having protected hydroxy groups
-
, (2008/06/13)
The present invention relates to compoun...
Compounds having protected hydroxy groups
-
, (2008/06/13)
The present invention relates to compoun...
Precursors for fragrant ketones and fragrant aldehydes
-
, (2008/06/13)
The present invention refers to fragranc...
14765-30-1 Process route
-
-
590-18-1
(Z)-2-Butene
-
-
21300-30-1
lithium 1-cyclohexenolate
-
-
14765-30-1
2-sec-butylcyclohexanone
-
-
71501-12-7
2,6-di(sec-butyl)cyclohexanone
| Conditions | Yield |
|---|---|
|
Yield given. Multistep reaction. Yields of byproduct given;
|
-
-
624-64-6
trans-2-Butene
-
-
21300-30-1
lithium 1-cyclohexenolate
-
-
14765-30-1
2-sec-butylcyclohexanone
-
-
71501-12-7
2,6-di(sec-butyl)cyclohexanone
| Conditions | Yield |
|---|---|
|
Yield given. Multistep reaction. Yields of byproduct given;
|
14765-30-1 Upstream products
-
34006-70-7
2,6-dibromocyclohexanone
-
91055-78-6
2-(1-methylpropylidene)cyclohexanone
-
590-18-1
(Z)-2-Butene
-
21300-30-1
lithium 1-cyclohexenolate
14765-30-1 Downstream products
-
144147-87-5
2-sec-Butyl-6-(2,2-dimethoxy-acetyl)-cyclohexanone
-
144148-32-3
7-sec-Butyl-2-(4-fluoro-phenyl)-4,5,6,7-tetrahydro-2H-indazole-3-carbaldehyde
-
144149-56-4
(E)-3-[7-sec-Butyl-2-(4-fluoro-phenyl)-4,5,6,7-tetrahydro-2H-indazol-3-yl]-propenal
-
162511-99-1
(E)-3-[7-sec-Butyl-2-(4-fluoro-phenyl)-4,5,6,7-tetrahydro-2H-indazol-3-yl]-prop-2-en-1-ol
