Welcome to LookChem.com Sign In|Join Free
  • or
Cyclohexanone, 4-(bromomethyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

197387-33-0

Post Buying Request

197387-33-0 Suppliers

Recommended suppliers

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

197387-33-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 197387-33-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,9,7,3,8 and 7 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 197387-33:
(8*1)+(7*9)+(6*7)+(5*3)+(4*8)+(3*7)+(2*3)+(1*3)=190
190 % 10 = 0
So 197387-33-0 is a valid CAS Registry Number.

197387-33-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-(bromomethyl)cyclohexan-1-one

1.2 Other means of identification

Product number -
Other names Cyclohexanone,4-(bromomethyl)

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:197387-33-0 SDS

197387-33-0Relevant academic research and scientific papers

Photoinduced Oxidation of Secondary Alcohols Using 4-Benzoylpyridine as an Oxidant

Kamijo, Shin,Tao, Keisuke,Takao, Go,Tonoda, Hiroshi,Murafuji, Toshihiro

supporting information, p. 3326 - 3329 (2015/07/15)

Photoinduced oxidation of secondary alcohols to ketones was achieved by utilizing an equimolar amount of 4-benzoylpyridine as an oxidant. This transformation proceeds at ambient temperature and exhibits high compatibility with polar functionalities including benzoyl, silyl, and methoxymethyl alcohol protecting groups as well as tosyloxy, bromo, sulfonyl, carbamate, ester, and carboxylic acid units. The present oxidation is solely promoted by the action of organic molecules without the aid of metallic reagents. (Chemical Equation Presented).

Structure-activity relationship of an ozonide carboxylic acid (oz78) against fasciola hepatica

Zhao, Qingjie,Vargas, Mireille,Dong, Yuxiang,Zhou, Lin,Wang, Xiaofang,Sriraghavan, Kamaraj,Keiser, Jennifer,Vennerstrom, Jonathan L.

experimental part, p. 4223 - 4233 (2010/09/04)

In this paper, we describe the SAR of ozonide carboxylic acid OZ78 (1) as the first part of our search for a trematocidal synthetic peroxide drug development candidate. We found that relatively small structural changes to 1 resulted most commonly in loss of activity against Fasciola hepatica in vivo. A spiroadamantane substructure and acidic functional group (or ester prodrug) were required for activity. Of 26 new compounds administered at single 100 mg/kg oral doses to F. hepatica infected rats, 8 had statistically significant worm burden reductions, 7 were partially curative, and 1 (acylsulfonamide 6) was completely curative and comparable to 1 in flukicidal efficacy. This study also showed that the activity of 1 is peroxide-bond-dependent, suggesting that its flukicidal efficacy depends upon hemoglobin digestion in F. hepatica.

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 197387-33-0