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Reputable factory supply 2,6-bis(4-chlorobenzylidene)cyclohexan-1-one 18989-82-7 in bulk at low price
- Molecular Formula: C20H16Cl2O
- Molecular Weight: 343.252
- Vapor Pressure: 2.91E-11mmHg at 25°C
- Melting Point: 147-148 °C
- Boiling Point: 528.7°Cat760mmHg
- Flash Point: 220.4°C
- PSA： 17.07000
- Density: 1.308g/cm3
- LogP: 6.21340
2,6-bis(4-chlorobenzylidene)cyclohexan-1-one(Cas 18989-82-7) Usage
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General Description |
2,6-bis(4-chlorobenzylidene)cyclohexan-1-one, also known as Muscone, is a synthetic compound commonly used in perfumery for its musky fragrance. It is a cyclic ketone with two benzylidene groups, each containing a chlorine atom, attached to the cyclohexane ring. Muscone is highly valued for its long-lasting and animalic scent, often described as sweet, woody, and musky. Due to its intense fragrance, it is used as a base note in many high-end perfumes and colognes. Additionally, it has been studied for its potential pharmaceutical properties, and it is also used as a flavoring agent in foods and beverages. |
InChI:InChI=1/C20H16Cl2O/c21-18-8-4-14(5-9-18)12-16-2-1-3-17(20(16)23)13-15-6-10-19(22)11-7-15/h4-13H,1-3H2
18989-82-7 Relevant articles
Design, synthesis and antimicrobial properties of novel 3,3a,4,5,6,7-hexahydroindazole and arylthiazolylpyrazoline derivatives
Bishnoi, Abha,Singh, Suruchi,Tiwari, Anil K.,Sethi, Arun,Tripathi, Chandrakant Mani
, p. 45 - 52 (2013)
A remarkable diastereoselective synthesi...
Activated charcoal-mediated synthesis of chalcones catalyzed by NaOH in water
Tanemura, Kiyoshi,Rohand, Taoufik
supporting information, (2021/02/27)
A variety of chalcones were synthesized ...
Synthesis of thiazolylidenethiazoloquinazolinone hybrids from monocarbonyl curcumin analogues. Characterization, bio-evaluation and DFT study
Benreka, Soufiane,Kasmi-Mir, Souad,Kirsch, Gilbert,Madi, Fatiha,Zradni, Fatima-Zohra
, (2021/09/03)
Given the diverse pharmacological attrib...
Synthesis and characterization of functionalized NaP Zeolite@CoFe2O4 hybrid materials: a micro–meso-structure catalyst for aldol condensation
Mortezaei, Zohreh,Zendehdel, Mojgan,Bodaghifard, Mohammad Ali
, p. 2169 - 2193 (2020/01/29)
In this work, magnetic nanocomposite of ...
Green, rapid, and highly efficient syntheses of α,α′-bis[(aryl or allyl)idene]cycloalkanones and 2-[(aryl or allyl)idene]-1-indanones as potentially biologic compounds via solvent-free microwave-assisted Claisen–Schmidt condensation catalyzed by MoCl5
Bakhshi, Reza,Zeynizadeh, Behzad,Mousavi, Hossein
, p. 623 - 637 (2019/08/26)
A new, green, and highly efficient proto...
18989-82-7 Process route
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-
6651-36-1
1-(Trimethylsilyloxy)cyclohexene
-
-
13086-93-6
(acetyloxy)(4-chlorophenyl)methyl acetate
-
-
18989-82-7,42792-80-3
(2E,6E)-2,6-bis(4-chlorobenzylidene)cyclohexanone
| Conditions | Yield |
|---|---|
|
With
boron trifluoride diethyl etherate;
In
diethyl ether; dichloromethane;
at 0 - 20 ℃;
|
49%
|
-
-
4-chlorobenzylidene dicrotonate
-
-
6651-36-1
1-(Trimethylsilyloxy)cyclohexene
-
-
18989-82-7,42792-80-3
(2E,6E)-2,6-bis(4-chlorobenzylidene)cyclohexanone
| Conditions | Yield |
|---|---|
|
With
boron trifluoride diethyl etherate;
In
diethyl ether; dichloromethane;
at 0 - 20 ℃;
|
30%
|
18989-82-7 Upstream products
-
108-94-1
cyclohexanone
-
104-88-1
4-chlorobenzaldehyde
-
1670-47-9
1,1-diethoxycyclohexane
-
6651-36-1
1-(Trimethylsilyloxy)cyclohexene
18989-82-7 Downstream products
-
110049-85-9
cis -2,6-bis-(4-chloro-benzyl)-cyclohexanone
-
6603-81-2
2,6-Bis- <4-chlor-benzyliden> -cyclohexan-1-ol
-
110049-85-9
2,6-bis(4-chlorobenzyl)cyclohexanone
-
54105-30-5
2-Amino-8(4-chlorbenzyliden)3-cyan-4(4-chlorphenyl)-5.6.7.8-tetrahydro-4-H-chromen
