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High Quality Chinese Manufacturer supply 3163-27-7 1-(Bromomethyl)naphthalene
- Molecular Formula: C11H9Br
- Molecular Weight: 221.096
- Appearance/Colour: off-white powder
- Vapor Pressure: 0.000422mmHg at 25°C
- Melting Point: 52-55 °C
- Refractive Index: 1.663
- Boiling Point: 326 °C at 760 mmHg
- Flash Point: 151.8 °C
- PSA： 0.00000
- Density: 1.444 g/cm3
- LogP: 3.73470
1-(Bromomethyl)naphthalene(Cas 3163-27-7) Usage
InChI:InChI=1/C11H9Br/c12-8-10-6-3-5-9-4-1-2-7-11(9)10/h1-7H,8H2
3163-27-7 Relevant articles
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Kritskaya et al.
, p. 103,113 (1971)
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Three-Component GaHal3-Promoted Reactions of Substituted Methylidenemalonates and Donor-Acceptor Cyclopropanes with Propargyl Halides: Cascade Diastereoselective Construction of Five-Membered Lactones
Denisov, Dmitry A.,Borisov, Denis D.,Korolev, Victor A.,Novikov, Roman A.,Tomilov, Yury V.
, p. 6174 - 6182 (2019)
A new cascade three-component process fo...
Identification of pheromone-like compounds in male reproductive organs of the oriental locust Locusta migratoria
Ban, Liping,Napolitano, Elio,Serra, Andrea,Zhou, Xianhong,Iovinella, Immacolata,Pelosi, Paolo
, p. 620 - 624 (2013)
Despite the great economical interest of...
-
Bullpitt et al.
, p. 760,762 (1976)
-
Photodecarboxylation of Substituted Naphthylmethyl Arylacetate Esters: Synthesis of Naphthylarylethanes
Hilborn, James W.,Moya-Barrios, Reinaldo,Thompson, Alison
, p. 11992 - 11999 (2019)
The synthesis of naphthylarylethanes via...
Antiproliferative activity of diarylnaphthylpyrrolidine derivative via dual target inhibition
Chanda, Debabrata,Dudi, Rajesh Kumar,Fatima, Kaneez,Iqbal, Hina,Khan, Feroz,Kumar, Yogesh,Luqman, Suaib,Mondhe, D. M.,Negi, Arvind S.,Shanker, Karuna,Tabassum, Misbah,Verma, Amit Kumar
, (2020)
Breast cancer is the second leading caus...
Preparation method of naphthalene ring C marked α .
-
Paragraph 0046-0047; 0050; 0056-0057; 0060; 0066-0067; 0070, (2021/10/05)
The invention discloses C labeled α - na...
Bioisosteric Modification of To042: Synthesis and Evaluation of Promising Use-Dependent Inhibitors of Voltage-Gated Sodium Channels
Milani, Gualtiero,Cavalluzzi, Maria Maddalena,Altamura, Concetta,Santoro, Antonella,Perrone, Mariagrazia,Muraglia, Marilena,Colabufo, Nicola Antonio,Corbo, Filomena,Casalino, Elisabetta,Franchini, Carlo,Pisano, Isabella,Desaphy, Jean-Fran?ois,Carrieri, Antonio,Carocci, Alessia,Lentini, Giovanni
, p. 3588 - 3599 (2021/10/07)
Three analogues of To042, a tocainide-re...
A mild method for the replacement of a hydroxyl group by halogen: 2. unified procedure and stereochemical studies
Gati, Wafa,Munyemana, Fran?ois,Colens, Alain,Srour, Aladdin,Dufour, Mathilde,Vardhan Reddy, K. Harsha,Téchy, Brigitte,Rosse, Gérard,Schweiger, Ed,Qiao, Qi,Ghosez, Léon
, (2020/08/19)
N,N-Dimethyl- and N,N-diisopropyl-1-halo...
3163-27-7 Process route
-
-
90-12-0,34475-76-8
1-Methylnaphthalene
-
-
6627-78-7
1-bromo-4-methylnaphthalene
-
-
3163-27-7
2-(bromomethyl)naphthalene
| Conditions | Yield |
|---|---|
|
With
N-Bromosuccinimide; dibenzoyl peroxide;
In
various solvent(s);
at 90 - 95 ℃;
for 1h;
|
73%
3% |
|
With
N-Bromosuccinimide;
at 150 ℃;
for 0.0666667h;
under 2625.26 Torr;
microwave irradiation;
|
53 % Chromat.
18 % Chromat. |
-
-
774197-63-6
3-(1-naphthylmethoxy)-3-bromoaziridine
-
-
90-12-0,34475-76-8
1-Methylnaphthalene
-
-
3163-27-7
2-(bromomethyl)naphthalene
| Conditions | Yield |
|---|---|
|
With
cyclohexa-1,4-diene;
In
chloroform;
at 20 ℃;
for 1h;
Further Variations:;
Reagents;
Product distribution;
UV-irradiation;
|
70 % Spectr.
30 % Spectr. |
3163-27-7 Upstream products
-
56-23-5
tetrachloromethane
-
128-08-5
N-Bromosuccinimide
-
90-12-0
1-Methylnaphthalene
-
50-00-0
formaldehyd
3163-27-7 Downstream products
-
6336-62-5
naphtho[2,1-b]quinolizinium bromide
-
109723-38-8
2-acetyl-1-[1]naphthylmethyl-pyridinium; bromide
-
114447-71-1
2-benzoyl-1-[1]naphthylmethyl-pyridinium; bromide
-
66969-01-5
5-ethyl-5-[1]naphthylmethyl-barbituric acid
