
879-18-5
- Product Name:1-Naphthoyl chloride
- Molecular Formula:C11H7ClO
- Purity:99%
- Molecular Weight:190.629
Product Details;
CasNo: 879-18-5
Molecular Formula: C11H7ClO
Appearance: Low melting solid/liquid
Excellent chemical plant bulk supply 1-Naphthoyl chloride 879-18-5
- Molecular Formula:C11H7ClO
- Molecular Weight:190.629
- Appearance/Colour:Low melting solid/liquid
- Vapor Pressure:0.00134mmHg at 25°C
- Melting Point:16-19 °C(lit.)
- Refractive Index:n20/D 1.652(lit.)
- Boiling Point:297.5 °C at 760 mmHg
- Flash Point:141.2 °C
- PSA:17.07000
- Density:1.271 g/cm3
- LogP:3.21880
1-Naphthoyl chloride(Cas 879-18-5) Usage
InChI:InChI=1/C11H7ClO/c12-11(13)10-7-3-5-8-4-1-2-6-9(8)10/h1-7H
879-18-5 Relevant articles
Palladium-Catalyzed Chlorocarbonylation of Aryl (Pseudo)Halides Through In Situ Generation of Carbon Monoxide
Bismuto, Alessandro,Boehm, Philip,Morandi, Bill,Roediger, Sven
supporting information, p. 17887 - 17896 (2020/08/19)
An efficient palladium-catalyzed chloroc...
Friedel–Crafts approach to the one-pot synthesis of methoxy-substituted thioxanthylium salts
Tanaka, Kenta,Tanaka, Yuta,Kishimoto, Mami,Hoshino, Yujiro,Honda, Kiyoshi
, p. 2105 - 2112 (2019/09/30)
An efficient synthesis of methoxy-substi...
Metathesis-active ligands enable a catalytic functional group metathesis between aroyl chlorides and aryl iodides
Lee, Yong Ho,Morandi, Bill
, p. 1016 - 1022 (2018/09/06)
Current methods for functional group int...
Functional Group Transposition: A Palladium-Catalyzed Metathesis of Ar-X σ-Bonds and Acid Chloride Synthesis
De La Higuera Macias, Maximiliano,Arndtsen, Bruce A.
supporting information, p. 10140 - 10144 (2018/08/23)
We describe the development of a new met...
879-18-5 Process route
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-
201230-82-2
carbon monoxide

-
-
90-14-2
1-Iodonaphthalene

-
-
879-18-5
naphthalene-1-carbonic acid chloride
Conditions | Yield |
---|---|
With
bis(tri-t-butylphosphine)palladium(0); benzyltriphenylphosphonium chloride;
In
toluene;
at 110 ℃;
for 24h;
under 38002.6 Torr;
Glovebox;
Autoclave;
Inert atmosphere;
|
98% |
-
-
79-37-8
oxalyl dichloride

-
-
86-55-5
1-naphthalenecarboxylic acid

-
-
879-18-5
naphthalene-1-carbonic acid chloride
Conditions | Yield |
---|---|
With
N,N-dimethyl-formamide;
In
dichloromethane;
at 0 - 20 ℃;
for 2h;
Inert atmosphere;
|
879-18-5 Upstream products
-
oxalyl dichloride
-
naphthalene
-
tetrachloromethane
-
iron(III) chloride
879-18-5 Downstream products
-
2-(naphthalen-1-yl)-N-phenylpropanamide
-
1-acetylamino-2-[1]naphthoyloxy-benzene
-
[1]naphthoic acid-(2-chloroacetyl-phenyl ester)
-
1-benzoylamino-2-[1]naphthoyloxy-benzene
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-
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-
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-
Adrenochrome
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