1-Benzyloxynaphthalene

Product Name: 1-Benzyloxynaphthalene
CAS No.: 607-58-9
Chemical Name: 1-Benzyloxynaphthalene
Synonyms: NSC 4044;1-Naphtylbenzyl ether;Naphthyl benzyl ether;Benzyl naphthyl ether;1-Benzyloxynaphthalene;(1-Naphtyl)benzyl ether;Benzyl 1-Naphthyl Ether;1-Naphthyl Benzyl Ether;9-(benzyloxy)phenanthrene;Benzyl alpha-naphthyl ether
CBNumber: CB31106517
Molecular Formula: C17H14O
Formula Weight: 234.29
MOL File: 607-58-9.mol

More

Less

1-Benzyloxynaphthalene Property

Melting point:: 73.5-74 °C
Boiling point:: 237-240 °C(Press: 13 Torr)
Density: 1.125±0.06 g/cm3(Predicted)
storage temp.: Sealed in dry,Room Temperature
solubility: Chloroform (Slightly), DMSO (Slightly), Ethyl Acetate (Slightly)
form: Solid
color: Pale Orange to Light Orange

More

Less

Hazard and Precautionary Statements (GHS)

Symbol(GHS)

Signal word

Danger

Hazard statements

H315Causes skin irritation

H318Causes serious eye damage

H335May cause respiratory irritation

H410Very toxic to aquatic life with long lasting effects

Precautionary statements

P261Avoid breathing dust/fume/gas/mist/vapours/spray.

P273Avoid release to the environment.

P280Wear protective gloves/protective clothing/eye protection/face protection.

P305+P351+P338IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continuerinsing.

More

Less

N-Bromosuccinimide Price

Sigma-Aldrich

Product number: S648094
Product name: BENZYL 1-NAPHTHYL ETHER
Purity: Aldrich<sup>CPR</sup>
Packaging: 1 unit
Price: $185
Updated: 2025/07/31

Sigma-Aldrich

Product number: S648094
Product name: BENZYL 1-NAPHTHYL ETHER
Purity: Aldrich
Packaging: 250mg
Price: $179
Updated: 2024/03/01

TRC

Product number: B286950
Product name: 1-(Benzyloxy)naphthalene
Packaging: 1g
Price: $545
Updated: 2021/12/16

American Custom Chemicals Corporation

Product number: CHM1047419
Product name: 1-(BENZYLOXY)NAPHTHALENE
Purity: 95.00%
Packaging: 5MG
Price: $495.53
Updated: 2021/12/16

AK Scientific

Product number: 4447BA
Product name: 1-(Benzyloxy)naphthalene
Packaging: 1g
Price: $243
Updated: 2021/12/16

More

Less

1-Benzyloxynaphthalene Chemical Properties,Usage,Production

Uses

1-Benzyloxynaphthalene is a naphthyl ether used in studies for the improvement of coal direct liquefaction by steam pretreatment.

Synthesis

90-15-3

100-39-0

28178-96-3

607-58-9

General procedure for the synthesis of compounds (CAS:28178-96-3) and 1-(benzyloxy)naphthalene from 1-naphthol and benzyl bromide: 0.14 g (1.0 mmol) of a mixture of 1-naphthol and 2-naphthol (1) and (6), mixed with 1.0 mmol of an alkali metal carbonate (0.14 g of K2CO3 or 0.33 g of Cs2CO3), was specified by 11.4 mg (0.05 mmol) of TEBAC and 1.2 mmol of alkyl halide (0.14 ml of benzyl bromide, 0.10 ml of ethyl iodide, 0.12 ml of butyl bromide, or 0.11 ml of isopropyl bromide) were added to a closed vial and reacted at 125°C for the appropriate reaction time using a 20-30 W light source or in a CEM Discover [300 W] microwave reactor. time. After completion of the reaction, the mixture was dissolved in 25 ml of ethyl acetate and the suspension was filtered. The volatile components were removed by evaporation to give the crude product. The crude product was initially purified by passing through a silica gel layer of about 2-3 cm thickness, using ethyl acetate as eluent, and the product was analyzed by GC-MS or GC. Similar reactions were carried out under 3 ml MeCN as solvent. The post-treatment step was similar to the solvent-free alkylation reaction described above, but in this case the addition of ethyl acetate was not necessary. Compounds 2, 7, 8, 10a-c and 13a, b can be obtained from the above reactions mainly in pure form by repetitive chromatography.Control experiments were carried out using benzyl bromide under conventional heating conditions with similar procedure.

References

[1] Letters in Organic Chemistry, 2013, vol. 10, # 5, p. 330 - 336

1-Benzyloxynaphthalene Preparation Products And Raw materials

Raw materials

Preparation Products

More

Less

1-Benzyloxynaphthalene Suppliers

Canada 1 China 27 India 1 United States 3 Global 32

J & K SCIENTIFIC LTD.

Tel: 18210857532; 18210857532
Fax: 86-10-82849933
Email: jkinfo@jkchemical.com
Country: China
ProdList: 96815
Advantage: 76

Chemsky (shanghai) International Co.,Ltd

Tel: 021-50135380
Email: shchemsky@sina.com
Country: China
ProdList: 15402
Advantage: 60

ShangHai KenEn Chemical Technology Co., Ltd.

Tel: 13120367189
Fax: 021-50315529
Email: mychess007@163.com
Country: China
ProdList: 1994
Advantage: 55

Aikon International Limited

Tel: 025-58859352 18068836627
Fax: 02557626880
Email: sales01@aikonchem.com
Country: China
ProdList: 16027
Advantage: 58

SHANGHAI FDC-CHEMICAL CO.,LTD

Tel: 021-61469567 13482353728
Fax: 021-61161605
Email: sales@fdc-chemical.com
Country: China
ProdList: 9721
Advantage: 58

Shenzhen Polymeri Biochemical Technology Co., Ltd.

Tel: +86-400-002-6226 +86-13028896684;
Email: sales@rrkchem.com
Country: China
ProdList: 57422
Advantage: 58

Shanghai TenSus Biotechnology Co., Ltd.

Tel: 021-50895067 18616507272
Fax: 021-50895067
Email: tensus@163.com
Country: China
ProdList: 8073
Advantage: 58

Beijing Haite lesk Technology Co., Ltd

Tel: 15210893940; 15116916250
Fax: QQ: 237008221
Email: chemistryliu@163.com
Country: China
ProdList: 7327
Advantage: 58

Shanghai Hecheng Medical Technology Co., LTD

Tel: 13564747822
Fax: QQ774046800
Email: 669027880@qq.com
Country: China
ProdList: 924
Advantage: 58

Energy Chemical

Tel: 021-58432009 400-005-6266
Fax: 021-58436166
Email: marketing@energy-chemical.com
Country: China
ProdList: 44918
Advantage: 58

TCI (Shanghai) Chemical Trading Co., Ltd.

Tel: 021-61109150
Fax: 021-61105897
Email: sales@tcisct.com
Country: China
ProdList: 29668
Advantage: 58

Hefei Mokai Pharmaceutical Technology Co., Ltd

Tel: 18130062233
Email: 3362556465@qq.com
Country: China
ProdList: 8100
Advantage: 58

Bide Pharmatech Ltd.

Tel: 400-6005915
Email: sales@picasso-e.com
Country: China
ProdList: 39653
Advantage: 58

Anhui Henuo Biotechnology Co., Ltd

Tel: 18455579438
Country: China
ProdList: 16684
Advantage: 58

Beijing Solarbio Science & Tecnology Co., Ltd.

Tel: 010-50973130 17801761073
Email: Gsiyu@solarbio.com
Country: China
ProdList: 50751
Advantage: 58

Shanghai Jieshikai Biotechnology Co. , Ltd.

Tel: 021-57520305 13795461237
Email: zhuruyan@jskchem.com
Country: China
ProdList: 49234
Advantage: 58

Accela ChemBio Co.,Ltd.

Tel: 021-50795510 4000665055
Email: SY06@accelachem.com
Country: China
ProdList: 7551
Advantage: 58

Yantai Shengkailun Chemical Technology Co., Ltd.

Tel: 13356901049
Email: mark@sklnchem.cn
Country: China
ProdList: 9993
Advantage: 58

Shanghai Ken chemical Technology Co.,ltd

Tel: 02152215958
Email: 47697177@qq.com
Country: China
ProdList: 10011
Advantage: 58

Merck KGaA

Tel: 21-20338288
Email: ordercn@merckgroup.com
Country: China
ProdList: 6394
Advantage: 58

Santa Cruz Biotechnology Inc

Tel: 021-60936350
Email: scbt@scbt.com
Country: China
ProdList: 6594
Advantage: 58

SHANGHAI KEAN TECHNOLOGY CO., LTD.

Tel: +8613817748580
Fax: 021-50175322
Email: cooperation@kean-chem.com
Country: China
ProdList: 40066
Advantage: 58

Shanghai Acmec Biochemical Technology Co., Ltd.

Tel: +86-18621343501; +undefined18621343501
Email: product@acmec-e.com
Country: China
ProdList: 33337
Advantage: 58

Henan Fengda Chemical Co., Ltd

Tel: +86-371-86557731 +86-13613820652
Fax: 86-0371-86557731
Email: info@fdachem.com
Country: China
ProdList: 20135
Advantage: 58

Hangzhou MolCore BioPharmatech Co.,Ltd.

Tel: +86-057181025280; +8617767106207
Fax: 0571-85806285
Email: sales@molcore.com
Country: China
ProdList: 49734
Advantage: 58

Shanghai Hao Zhun Biological Technology Co., Ltd.

Tel: --
Fax: --
Email: info@zzsrm.com
Country: CHINA
ProdList: 6650
Advantage: 58

More

Less

View Lastest Price from 1-Benzyloxynaphthalene manufacturers

Henan Fengda Chemical Co., Ltd

Product: 1-Benzyloxynaphthalene 607-58-9
Price: US $101.00-1.00/KG
Min. Order: 1KG
Purity: 99%
Supply Ability: g-kg-tons, free sample is available
Release date: 2023-12-28

607-58-9, 1-BenzyloxynaphthaleneRelated Search:

Elsamitrucin CHARTREUSIN α-Naphthoflavone Benzyl ether 1-naphthyl benzoate 1-Benzyloxynaphthalene ALPHA-NAPHTHOFLAVANONE 6H-Benzo(d)naphtho(1,2-b)pyran-6-one, 4-(6-deoxy-alpha-galactofuranosy l)-1-hydroxy-10,12-dimethoxy-8-methyl- 12-((6-Deoxyhexopyranosyl)oxy)-1,10-dihydroxy-8-methyl-6H-benzo(d)naph tho(1,2-b)pyran-6-one A-NAPHTHOFLAVONOL ravidomycin desacetylravidomycin 1-[1-(BENZYLOXY)-2-NAPHTHYL]-3-(1-NAPHTHYL)PROP-2-EN-1-ONE 2'-HYDROXY-ALPHA-NAPHTHOFLAVONE 3',4'-DIMETHOXY-ALPHA-NAPHTHOFLAVONE 1-[1-(BENZYLOXY)-2-NAPHTHYL]-3-PHENYLPROP-2-EN-1-ONE ETHYL 5-[(4-FLUOROBENZOYL)OXY]-1,2-DIMETHYL-1H-BENZO[G]INDOLE-3-CARBOXYLATE 2'-METHOXY-7,8-BENZOFLAVONE

1-Benzyloxynaphthalene

Benzyl naphthyl ether

Naphthyl benzyl ether

Benzyl alpha-naphthyl ether

1-(PHENYLMETHOXY)NAPHTHALENE

(1-Naphtyl)benzyl ether

1-Naphtylbenzyl ether

1-Naphthyl Benzyl Ether

Benzyl 1-Naphthyl Ether

NSC 4044

Naphthalene, 1-(phenylmethoxy)-

9-(benzyloxy)phenanthrene

607-58-9

Aromatics

Intermediates & Fine Chemicals

Pharmaceuticals