Welcome to LookChem.com Sign In|Join Free

CAS

  • or

36960-03-9

Post Buying Request

36960-03-9 Suppliers

Recommended suppliersmore

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

36960-03-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 36960-03-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,6,9,6 and 0 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 36960-03:
(7*3)+(6*6)+(5*9)+(4*6)+(3*0)+(2*0)+(1*3)=129
129 % 10 = 9
So 36960-03-9 is a valid CAS Registry Number.

36960-03-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-oxo-3-phenylpropyl acetate

1.2 Other means of identification

Product number -
Other names 1-Acetoxy-3-phenyl-aceton

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:36960-03-9 SDS

36960-03-9Relevant articles and documents

Regioselective Wacker-Type Oxidation of Internal Olefins in tBuOH Using Oxygen as the Sole Oxidant and tBuONO as the Organic Redox Cocatalyst

Huang, Qing,Li, Ya-Wei,Ning, Xiao-Shan,Jiang, Guo-Qing,Zhang, Xiao-Wei,Qu, Jian-Ping,Kang, Yan-Biao

, p. 965 - 969 (2020/02/15)

A regioselective Wacker-Tsuji oxidation of internal olefins in tBuOH has been developed using oxygen as the terminal oxidant and tert-butyl nitrite as the simple organic redox cocatalyst without the involvement of hazardous cocatalysts or harsh reaction conditions. A series of internal olefins bearing various functional groups can be oxidized to the corresponding substituted ketones in generally good yields with high regioselectivities.

Synthesizing method of alpha-arone or alpha-hetero-arone

-

, (2018/09/08)

The invention discloses a synthesizing method of alpha-arone or alpha-hetero-arone and belongs to the technical field of metal organic catalyzing. The synthesizing method has the advantages that a terminal alkynyl compound, oxynitride and a proton supply agent is catalyzed by univalence metal salt to obtain N-O pyridine oxynitride enol salt, purification and separation are not needed, and the N-Opyridine oxynitride enol salt is allowed to have reaction with arene and hetero-arene in a one-pot manner to obtain the alpha-arone or alpha-hetero-arone; the method is high in functional group tolerance, wide in substrate application range, high in yield, simple and easy to operate and easy in final product separation and purification.

Methods and Compositions for Treatment of Scleritis and Related Disorders

-

Page/Page column 29-32, (2008/12/05)

The present teachings relate to the field of anti-inflammatory substances and more particularly to compounds that are useful for the treatment of scleritis, a scleritis symptom, or a scleritis-related disorder. In one aspect, methods of treating scleritis, a scleritis symptom, or a scleritis-related disorder generally include administering to a subject a compound of Formula I: or a pharmaceutically acceptable salt, hydrate or ester thereof, wherein W1, W2, R1, L, X, Y, Z, and n1 are defined as described herein.

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 36960-03-9