Welcome to LookChem.com Sign In|Join Free
  • or
2,7-Diethoxynaphthalene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

70708-31-5

Post Buying Request

70708-31-5 Suppliers

Recommended suppliers

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

70708-31-5 Usage

Physical state

Pale yellow solid

Odor

Naphthalene-like

Solubility

Sparingly soluble in water

Usage

Precursor for the synthesis of various organic compounds, reagent in organic chemistry, versatile building block in the production of pharmaceuticals, dyes, and agrochemicals

Potential applications

Organic electronics and optoelectronics

Safety precautions

May pose health hazards if not properly managed

Check Digit Verification of cas no

The CAS Registry Mumber 70708-31-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,0,7,0 and 8 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 70708-31:
(7*7)+(6*0)+(5*7)+(4*0)+(3*8)+(2*3)+(1*1)=115
115 % 10 = 5
So 70708-31-5 is a valid CAS Registry Number.

70708-31-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,7-diethoxynaphthalene

1.2 Other means of identification

Product number -
Other names Naphthalene,2,7-diethoxy

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:70708-31-5 SDS

70708-31-5Downstream Products

70708-31-5Relevant academic research and scientific papers

Catalytic asymmetric hydrogenation of naphthalenes

Kuwano, Ryoichi,Morioka, Ryuichi,Kashiwabara, Manabu,Kameyama, Nao

supporting information; experimental part, p. 4136 - 4139 (2012/06/01)

Vanishing aromaticity: A chiral ruthenium complex catalyzes the hydrogenation of 2,6- or 2,7-disubstituted naphthalenes to give chiral tetralins with up to 92 % ee. The chiral catalyst is applicable to the regio- and enantioselective reduction of 6-substi

Facile Cleavage of Aryl Haloacetates and 2-Chloroethyl Carboxylic Esters with Sodium Telluride. A One-pot Conversion of Aryl Eters into Aryl Esthers under Aprotic Conditions

Suzuki, Hitomi,Padmanabhan, Seetharamaiyer,Ogawa, Takuji

, p. 1017 - 1020 (2007/10/02)

Sodium telluride, prepared under aprotic conditions, cleaved aryl haloacetates and 2-chloroethyl carboxylates at room temperature to give phenolic compounds and carboxylic acids, respectively.Based on this cleavage a one-pot conversion of aryl esters into aryl ethers was achieved.

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1 Customer Service

What can I do for you?
Get Best Price

Get Best Price for 70708-31-5