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1599-67-3

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1599-67-3 Usage

Uses

Different sources of media describe the Uses of 1599-67-3 differently. You can refer to the following data:
1. Antiviral used in the treatment of herpes simplex labialis.
2. 1-Docosene is a long-chain alkene and one of the lipophilic components of the aerial parts of the plant Origanum vulgare. A useful building block.

Definition

ChEBI: An alkene that is docosane with an unsaturation at position 1. Metabolite observed in cancer metabolism.

Brand name

Abreva (GlaxoSmithKline) [Note—The International Cosmetic Ingredient (ICNI) name for docosanol is behenyl alcohol.].

Check Digit Verification of cas no

The CAS Registry Mumber 1599-67-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,5,9 and 9 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1599-67:
(6*1)+(5*5)+(4*9)+(3*9)+(2*6)+(1*7)=113
113 % 10 = 3
So 1599-67-3 is a valid CAS Registry Number.
InChI:InChI=1/C22H46O/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-18-19-20-21-22-23/h23H,2-22H2,1H3

1599-67-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 10, 2017

Revision Date: Aug 10, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-docosene

1.2 Other means of identification

Product number -
Other names 1-DOCOSANOL

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only. Lubricants and lubricant additives,Viscosity adjustors
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:1599-67-3 SDS

1599-67-3Relevant articles and documents

-

Sharpless,K.B.,Flood,T.C.

, p. 370 - 371 (1972)

-

Phase-Transfer Synthesis of Monoalkyl Ethers of Oligoethylene Glycols

Gibson, Thomas

, p. 1095 - 1098 (2007/10/02)

The effects of catalyst, temperature, solvent, and reagent ratios on the phase-transfer-catalyzed Williamson ether synthesis of monoalkyl ethers of oligoethylene glycols have been studied.A convenient method has been developed which gives reproducibly high yields of pure monoethers in the presence of aqueous sodium hydroxide.

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