Welcome to LookChem.com Sign In|Join Free
  • or
Benzene, 1,1'-[nonylidenebis(thio)]bis- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

113138-70-8

Post Buying Request

113138-70-8 Suppliers

Recommended suppliers

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

113138-70-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 113138-70-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,3,1,3 and 8 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 113138-70:
(8*1)+(7*1)+(6*3)+(5*1)+(4*3)+(3*8)+(2*7)+(1*0)=88
88 % 10 = 8
So 113138-70-8 is a valid CAS Registry Number.

113138-70-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-phenylsulfanylnonylsulfanylbenzene

1.2 Other means of identification

Product number -
Other names Benzene,1,1'-[nonylidenebis(thio)]bis

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:113138-70-8 SDS

113138-70-8Downstream Products

113138-70-8Relevant academic research and scientific papers

ACTIVATION AND SYNTHETIC APPLICATIONS OF THIOSTANNANES. THIOALKOXYLATION OF ACETALS

Sato, Tsuneo,Otera, Junzo,Nozaki, Hitosi

, p. 1209 - 1218 (2007/10/02)

The Sn-S bonds in thiostannanes, BunSn(SPh)4-n, are activated towards acetals in the presence of BF3*OEt2.Acetals of various aldehydes and ketones are converted into the corresponding monothioacetals under mild conditions.Employment of α-enal acetals induces Michael addition to give synthetically useful γ-alkoxyally sulfides.

Organotin-Mediated Preparation of Monothioacetals

Sato, Tsuneo,Kobayashi, Takamitsu,Gojo, Tamehisa,Yoshida, Enji,Otera, Junzo,Nozaki, Hitosi

, p. 1661 - 1664 (2007/10/02)

Monothioacetals are obtained by treating the corresponding acetals with organotin thiophenoxides in the presence of BF3*OEt2.The reaction proceeds under mild conditions to provide the desired compounds with high selectivity.

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 113138-70-8