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56484-51-6

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56484-51-6 Usage

Appearance

White crystalline solid

Uses

a. Production of perfumes
b. Flavorings
c. Pharmaceuticals

Fragrance industry application

Fixative to enhance longevity and stability of scents

Odor

Pleasant floral

Synthesis

Used in the synthesis of organic compounds

Chemical reactions

Used as a starting material for various chemical reactions

Safety precautions

a. Can irritate eyes and skin
b. Prolonged exposure may cause adverse health effects
c. Handle with care

Check Digit Verification of cas no

The CAS Registry Mumber 56484-51-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,6,4,8 and 4 respectively; the second part has 2 digits, 5 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 56484-51:
(7*5)+(6*6)+(5*4)+(4*8)+(3*4)+(2*5)+(1*1)=146
146 % 10 = 6
So 56484-51-6 is a valid CAS Registry Number.

56484-51-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-ethyl-2-phenyl-1,3-benzodioxole

1.2 Other means of identification

Product number -
Other names .2-Aethyl-2-phenyl-1,3-benzodioxol

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:56484-51-6 SDS

56484-51-6Relevant articles and documents

Ru3(CO)12-catalyzed reactions of catechols with alkynes: An atom-economic process for the synthesis of 2,2-disubstituted 1,3-benzodioxoles from the double addition of the O-H bond across a triple bond

Li, Ming,Hua, Ruimao

supporting information; experimental part, p. 8658 - 8660 (2009/04/11)

(Chemical Equation Presented) Ru3(CO)12 has been found to be the efficient catalyst for the addition reactions of catechols with both terminal and internal alkynes to selectively afford 2,2-disubstituted 1,3-benzodioxoles in good to high yields. The formation of 2,2-substituted 1,3-benzodioxoles results from the tandem addition of two O-H bonds of catechols to alkyne's triple bond.

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