Welcome to LookChem.com Sign In|Join Free

CAS

  • or

4705-32-2

Post Buying Request

4705-32-2 Suppliers

Recommended suppliersmore

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

4705-32-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4705-32-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,7,0 and 5 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 4705-32:
(6*4)+(5*7)+(4*0)+(3*5)+(2*3)+(1*2)=82
82 % 10 = 2
So 4705-32-2 is a valid CAS Registry Number.

4705-32-2SDS

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 1-ethoxy-4-[2-(4-ethoxyphenyl)ethenyl]benzene

1.2 Other means of identification

Product number -
Other names 1,10-Bis[4-(ethoxycarbonyl)phenoxy]decane

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:4705-32-2 SDS

4705-32-2Downstream Products

4705-32-2Relevant articles and documents

COLORING COMPOSITION AND RECORDING METHOD

-

Paragraph 0094, (2018/03/23)

PROBLEM TO BE SOLVED: To provide a coloring composition that can form an image having silver gloss. SOLUTION: A coloring composition contains a stilbene compound represented by general formula (1), and two or more solvents. For the two or more solvents, a

Organometallic Compounds: Part I - Reduction of Benzophenones, 4,4'-Dialkoxydeoxybezoins, Benzils and Chalkones with Cyclohexylmethylmagnesium Bromide

Habashi, Abida,Tadros, Wadie,Shams, Hoda Zaki

, p. 659 - 662 (2007/10/02)

Cyclohexylmethylmagnesium bromide (I) reduces benzophenones (IIa-e) when reacted in a molar ratio of 4:1, to give mainly the corresponding benzhydrols (IIIa-e).A similar reaction of I with 4,4'-dialkoxydeoxybenzoins (IIf,g) results in the formation of carbinols (IIIf,g), the dehydration of which gives the corresponding stilbenes (VIIa,b).However, when benzil (IXa) (1 mol) is treated with I (4 mol), both reduction and addition reactions take place giving rise to a mixture of benzoin (Xa) and the addition product (IXa).A similar reaction of I with 4,4'-dimethoxybenzil (IXb) gives the addition product (XIb) together with anisic acid.

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

What can I do for you?
Get Best Price

Get Best Price for 4705-32-2