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  • 37951-47-6 Structure
  • Basic information

    1. Product Name: 3-benzyloxypropiophenone
    2. Synonyms: 3-benzyloxypropiophenone;1-(3-benzyloxyphenyl)propan-1-one;1-(3-Benzyloxyphenyl)-1-propanone;1-[3-(PhenylMethoxy)phenyl]-1-propanone;M-(Benzyloxy)-propiophenone
    3. CAS NO:37951-47-6
    4. Molecular Formula: C16H16O2
    5. Molecular Weight: 240.29704
    6. EINECS: N/A
    7. Product Categories: Aromatics;Intermediates
    8. Mol File: 37951-47-6.mol
    9. Article Data: 2
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: -20°C Freezer
    8. Solubility: Dichloromethane, Ethyl Acetate, Methanol
    9. CAS DataBase Reference: 3-benzyloxypropiophenone(CAS DataBase Reference)
    10. NIST Chemistry Reference: 3-benzyloxypropiophenone(37951-47-6)
    11. EPA Substance Registry System: 3-benzyloxypropiophenone(37951-47-6)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 37951-47-6(Hazardous Substances Data)

37951-47-6 Usage

Description

3-Benzyloxypropiophenone is an organic compound that exists as a colorless oil. It serves as a crucial intermediate in the synthesis of various pharmaceutical products, including ectoparasiticides, drug metabolites, and analgesic agents.

Uses

Used in Pharmaceutical Industry:
3-Benzyloxypropiophenone is used as an intermediate for the production of various ectoparasiticides, which are substances that help in the treatment and prevention of ectoparasites, such as lice and ticks. Its role in the synthesis of these agents is crucial for their effectiveness in controlling and eliminating these parasites.
Additionally, 3-benzyloxypropiophenone is used as an intermediate in the synthesis of drug metabolites. These metabolites are the products of the body's metabolism of drugs, which can sometimes have therapeutic effects or may be inactive or even toxic. 3-benzyloxypropiophenone's involvement in their production is essential for understanding the pharmacokinetics and pharmacodynamics of various medications.
Furthermore, 3-benzyloxypropiophenone is utilized as an intermediate in the creation of analgesic agents, which are substances that help alleviate pain. Its role in the synthesis of these pain-relieving drugs is vital for their effectiveness in providing relief to patients suffering from various types of pain.

Check Digit Verification of cas no

The CAS Registry Mumber 37951-47-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,7,9,5 and 1 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 37951-47:
(7*3)+(6*7)+(5*9)+(4*5)+(3*1)+(2*4)+(1*7)=146
146 % 10 = 6
So 37951-47-6 is a valid CAS Registry Number.

37951-47-6SDS

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 1-(3-phenylmethoxyphenyl)propan-1-one

1.2 Other means of identification

Product number -
Other names 3-benzyloxypropiophenone

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:37951-47-6 SDS

37951-47-6Relevant articles and documents

Studies of the new herbicide KIH-6127. Part II. Synthesis and herbicidal activity of 6-acyl pyrimidin-2-yl salicylates and analogues against barnyard grass

Tamaru,Takehi,Masuyama,Hanai

, p. 327 - 335 (2007/10/03)

The method reported previously (Part I) was employed to prepare a variety of novel 6-acylsalicylates as key intermediates. 6-Acylpyrimidin-2- yl salicylates (2-acyl-6-[(4,6-disubstituted pyrimidin-2-yl)oxy]benzoate derivatives: Type 1), the closely relate

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