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methyl 2-(naphthalen-1-yl)benzoate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 93655-02-8 Structure
  • Basic information

    1. Product Name: methyl 2-(naphthalen-1-yl)benzoate
    2. Synonyms:
    3. CAS NO:93655-02-8
    4. Molecular Formula: C18H14O2
    5. Molecular Weight: 262.3026
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 93655-02-8.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 415.1°C at 760 mmHg
    3. Flash Point: 188.7°C
    4. Appearance: N/A
    5. Density: 1.156g/cm3
    6. Vapor Pressure: 4.24E-07mmHg at 25°C
    7. Refractive Index: 1.627
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. CAS DataBase Reference: methyl 2-(naphthalen-1-yl)benzoate(CAS DataBase Reference)
    11. NIST Chemistry Reference: methyl 2-(naphthalen-1-yl)benzoate(93655-02-8)
    12. EPA Substance Registry System: methyl 2-(naphthalen-1-yl)benzoate(93655-02-8)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 93655-02-8(Hazardous Substances Data)

93655-02-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 93655-02-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,3,6,5 and 5 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 93655-02:
(7*9)+(6*3)+(5*6)+(4*5)+(3*5)+(2*0)+(1*2)=148
148 % 10 = 8
So 93655-02-8 is a valid CAS Registry Number.

93655-02-8SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name methyl 2-naphthalen-1-ylbenzoate

1.2 Other means of identification

Product number -
Other names -

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:93655-02-8 SDS

93655-02-8Relevant articles and documents

Non-c2-symmetric bis-benzimidazolium salt applied in the synthesis of sterically hindered biaryls

Chen, Yen-Hsin,Hsu, Tung-Yu,Huang, Shu-Jyun,Hung, Pei-Yu,Lee, Dong-Sheng,Lu, Ta-Jung,Wei, Ting-Rong

, (2021/11/27)

A novel non-C2-symmetric bis-benzimidazolium salt derived from (±)-valinol has been prepared by a simple and straightforward process in good yield. The structure of bis-benzimidazolium salt provided a bulky steric group on the ethylene bridge; which facilitates the catalytic efficacy in the C(sp2 )–C(sp2 ) formation. Its catalytic activity in Suzuki–Miyaura cross-coupling reaction of unactivated aryl chlorides has been found to have high efficacy in 1 mol% Pd loading. This protocol demonstrated the potential on the synthesis of sterically hindered biaryls.

AROMATIC AMINE DERIVATIVE AND ORGANIC ELECTROLUMINESCENT DEVICE COMPRISING SAME

-

Paragraph 0193-0198, (2021/04/20)

The present invention relates to an organic light emitting compound which is aromatic amine derivatives expressed as chemical formula A and has excellent light emitting properties such as brightness and light emitting efficiency compared with those of an existing light emitting material. Accordingly, an organic electroluminescent device comprising the same has excellent light emitting properties.

AROMATIC AMINE DERIVATIVE AND ORGANIC ELECTROLUMINESCENT DEVICE COMPRISING SAME

-

Paragraph 0159-0163, (2021/05/18)

The present invention is an organic light emitting compound characterized by an aromatic amine derivative represented by chemical formula A. The aromatic amine derivative has excellent light emitting properties such as brightness, luminous efficiency, etc

Synthesis of seven-membered lactones by regioselective and stereoselective iodolactonization of electron-deficient olefins

Ke, Zhuofeng,Li, Ming,Liu, Yue-Jin,Luo, Xiao-Peng,Shao, You-Xiang,Tang, Pan-Ting,Wang, Liang-Neng,Wei, Yi,Zeng, Ming-Hua,Zhang, Ni-Juan

supporting information, p. 6680 - 6683 (2020/07/03)

A regio- A nd stereoselective iodolactonization of internal electron-deficient olefinic acids has been reported, which provides a straightforward access to a series of multi-functionalized seven-membered lactones containing two consecutive chiral centers. The ester substituents on the olefins played a key role in achieving high regioselectivity. This result was proved through experiments and DFT calculations.

Visible-Light-Induced Arene C(sp 2)-H Lactonization Promoted by DDQ and tert -Butyl Nitrite

Chen, Bajin,Hu, Baoxiang,Hu, Xinquan,Jin, Liqun,Li, Meichao,Shen, Zhenlu,Sun, Nan,Wang, Shengpeng,Wang, Yiqing

supporting information, p. 261 - 266 (2020/02/18)

A visible-light photocatalytic aerobic oxidative lactonization of arene C(sp 2)-H bonds proceeds in the presence of 2,3-dichloro-5,6-dicyano-1,4-benzoquinone (DDQ) and tert -butyl nitrite (TBN). Under the optimized conditions, a range of 2-arylbenzoic acids is converted into the corresponding benzocoumarin derivatives in moderate to excellent yields. This method is characterized by its atom economy, mild reaction conditions, the use of a green oxidant and metal-free catalysis.

Exploration of Biaryl Carboxylic Acids as Proton Shuttles for the Selective Functionalization of Indole C-H Bonds

Pi, Jing-Jing,Lu, Xiao-Yu,Liu, Jing-Hui,Lu, Xi,Xiao, Bin,Fu, Yao,Guimond, Nicolas

, p. 5791 - 5800 (2018/05/14)

A survey of diversely substituted 2-arylbenzoic acids were synthesized and tested for use as proton shuttle in the direct arylation of indoles with bromobenzenes. It was found that 3-ethoxy-2-phenylbenzoic acid gives superior yield and selectivity for this class of substrates.

Differentially Substituted Phosphines via Decarbonylation of Acylphosphines

Yu, Rongrong,Chen, Xingyu,Martin, Stephen F.,Wang, Zhiqian

, p. 1808 - 1811 (2017/04/11)

A new route to phosphines was developed by a method that features a "pre-join and transform" process that proceeds via acylphosphine intermediates that may be readily prepared from carboxylic acids and disubstituted phosphines. The efficient decarbonylations of these acylphosphines using a nickel catalyst delivered the corresponding phosphines. This method shows that the carboxyl group can play a role similar to halides or triflates for introducing a substituted phosphorus atom on an aromatic ring.

Aromatic amine luminous compound and organic electroluminescence device manufactured through same

-

Paragraph 0049; 0050; 0051, (2016/10/09)

The invention provides an aromatic amine luminous compound. The aromatic amine luminous compound has good heat stability, high luminous efficiency and high luminous purity, and can be used for manufacturing an organic electroluminescence device and applied to the field of organic solar cells or organic thin-film transistors or organic photoreceptors. The invention further provides the organic electroluminescence device which comprises an anode, a cathode and an organic layer. The organic layer comprises one or more of a luminous layer, a hole injection layer, a hole transfer layer, a hole blocking layer, an electron injection layer and an electron transfer layer. At least one layer in the organic layer comprises the compound shown in the structural formula I shown in the description.

A kind of organic compound and its use this organic compound electroluminescent device

-

Paragraph 0035-0037;0038, (2016/10/08)

The invention relates to an organic compound. The organic compound has a structure represented in a formula I, wherein R1, R2 and R3 are independently selected from hydrogen atom, substituted or non-substituted C1-C30 alkyl, substituted or non-substituted C1-C30 naphthenic base, substituted or non-substituted C1-C30 alkoxy, substituted or non-substituted C6-C30 aryl, substituted or non-substituted C6-C30 aryloxy, substituted or non-substituted C6-C30 arylamine, substituted or non-substituted C2-C30 heterocyclic ring, substituted or non-substituted C6-C30 condensed polycyclic group, hydroxyl, cyano group and substituted or non-substituted amino, respectively. Furthermore, the invention relates to an electroluminescent device, wherein the electroluminescent device comprises a hole injection layer and/or a hole transport layer using at least one of the compounds.

Using this new organoelectroluminescent compound and an organic electroluminescence element

-

Paragraph 0041, (2016/10/08)

Disclosed are novel organic electroluminescent compounds and organic electroluminescent devices comprising the same. With good luminous efficiency and excellent color purity and life property, the organic electroluminescent compounds according to the inve

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