Welcome to LookChem.com Sign In|Join Free

CAS

  • or

13702-07-3

Post Buying Request

13702-07-3 Suppliers

Recommended suppliersmore

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

13702-07-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 13702-07-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,7,0 and 2 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 13702-07:
(7*1)+(6*3)+(5*7)+(4*0)+(3*2)+(2*0)+(1*7)=73
73 % 10 = 3
So 13702-07-3 is a valid CAS Registry Number.

13702-07-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name but-2-ynylselanylbenzene

1.2 Other means of identification

Product number -
Other names 1-Phenylseleno-but-2-in

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:13702-07-3 SDS

13702-07-3Relevant articles and documents

General synthesis of alkyl phenyl selenides from organic halides mediated by zinc in aqueous medium

Bieber, Lothar W.,De Sá, Ana C.P.F.,Menezes, Paulo H.,Gon?alves, Simone M.C.

, p. 4597 - 4599 (2007/10/03)

Organic halides of different structural types react with diphenyl diselenide and zinc dust in aqueous medium to give alkyl phenyl selenides. Benzylic and allylic bromides, α-bromoesters, acids and ketones and some primary alkyl iodides produce high yields even under acidic conditions. Less reactive halides need basic medium. The reaction proceeds equally well in the presence of various unprotected functional groups. Control experiments support a SH2 mechanism via alkyl radicals.

SELECTIVE ONE-POT SYNTHESIS OF ALLENYL PHENYL SELENIDE AND 1-(PHENYLSELENO)PROPYNE. ROLE OF SODIUM BENZENESELENOLATE AS A BASE IN DMF

Saito, Seiki,Hamano, Shin-ichi,Inaba, Masami,Moriwake, Toshio

, p. 1105 - 1110 (2007/10/02)

The reaction of excess sodium benzeneselenolate with propargyl bromide in DMF-THF at room temperature produced allenyl phenyl selenide or 1-(phenylseleno)propyne selectively, depending only on the reaction time.

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 13702-07-3