Welcome to LookChem.com Sign In|Join Free

CAS

  • or

4675-57-4

Post Buying Request

4675-57-4 Suppliers

Recommended suppliersmore

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

4675-57-4 Usage

Type of fatty acid

Monounsaturated omega-7 fatty acid

Natural sources

Macadamia nuts, salmon, and spinach

Essentiality

Not considered an essential fatty acid, as the human body can produce it in small amounts

Health benefits

Potentially reduces inflammation, improves insulin sensitivity, promotes cardiovascular health, and maintains skin health

Role in skin

Component of the skin's natural sebum

Research status

Ongoing, with potential therapeutic applications being investigated

Check Digit Verification of cas no

The CAS Registry Mumber 4675-57-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,6,7 and 5 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 4675-57:
(6*4)+(5*6)+(4*7)+(3*5)+(2*5)+(1*7)=114
114 % 10 = 4
So 4675-57-4 is a valid CAS Registry Number.

4675-57-4SDS

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 hexadec-15-enoic acid

1.2 Other means of identification

Product number -
Other names 15-Hexadecenoic acid

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:4675-57-4 SDS

4675-57-4Relevant articles and documents

Synthesis of ω-Unsaturated Acids

Mirviss, Stanley B.

, p. 1948 - 1951 (2007/10/02)

A short, high-yield method for the synthesis of ω-unsaturated acids have been developed that precludes any double-bond migration or hydrogenation.Key is the coupling reaction between Grignards of ω-unsaturated alkyl halides and the bromomagnesium salt of ω-bromo fatty acids.The reaction has been successfully extended to ω-bromo nitriles.The use of ω-chloro acids or α-bromo acids gives lower yields of heterocoupling products and substantial homocoupling.A catalyst study shows Li2CuCl4 to yield the most heterocoupling of several catalysts tried for the chloro acids, and Ni(II) or Cu(I) are best for the α-bromo acids.

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 4675-57-4