Welcome to LookChem.com Sign In|Join Free
  • or
N-thiobenzoyl benzamidine is a chemical compound with the molecular formula C14H12N2OS. It is a derivative of benzamidine, which is a benzene ring with an amide group attached to it. The "N-thiobenzoyl" part of the name indicates that a thiobenzoyl group (a benzoyl group with a sulfur atom replacing one of the oxygen atoms) is attached to the nitrogen atom of the benzamidine. N-thiobenzoyl benzamidine is often used in the synthesis of various pharmaceuticals and agrochemicals due to its reactivity and ability to form stable intermediates. It is also known for its potential applications in the development of new materials and as a building block in organic chemistry.

4115-33-7

Post Buying Request

4115-33-7 Suppliers

Recommended suppliers

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

4115-33-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4115-33-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,1,1 and 5 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 4115-33:
(6*4)+(5*1)+(4*1)+(3*5)+(2*3)+(1*3)=57
57 % 10 = 7
So 4115-33-7 is a valid CAS Registry Number.

4115-33-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name N-thiobenzoyl benzamidine

1.2 Other means of identification

Product number -
Other names Benzimidoyl-thiobenzoyl-amin

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:4115-33-7 SDS

4115-33-7Relevant academic research and scientific papers

Aerobic Visible-Light Induced Intermolecular S?N Bond Construction: Synthesis of 1,2,4-Thiadiazoles from Thioamides under Photosensitizer-Free Conditions

Wang, Hui,Xie, Shihua,Zhu, Hongjun,Zhuo, Liang

supporting information, p. 3398 - 3402 (2021/06/25)

Aerobic visible-light induced intermolecular S?N bond construction has been achieved without the addition of photosensitizer, metal, or base. With this strategy, 1,2,4-thiadiazoles can be obtained from thioamides. Preliminary mechanistic investigation suggested that the excited state of thioamides undergoes a single-electron-transfer (SET) process to afford thioamidyl radicals, which can be further transformed into a 1,2,4-thiadiazole through desulfurization and oxidative cyclization. The reaction has good functional group tolerance and represents a green method for the construction of S?N bonds.

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 4115-33-7