Welcome to LookChem.com Sign In|Join Free

CAS

  • or

4706-81-4

Post Buying Request

4706-81-4 Suppliers

Recommended suppliersmore

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

4706-81-4 Usage

Description

2-Tetradecanol, also known as ChEBI, is a fatty alcohol derived from tetradecane with a hydroxy group substitution at the 2nd position. It is characterized by its white powder appearance and is known for its unique chemical properties.

Uses

Used in Diagnostics Industry:
2-Tetradecanol is used as a diagnostic aid for identifying bacterial infections in wounds. Its properties allow for the effective detection and monitoring of bacterial presence, contributing to the accurate diagnosis and subsequent treatment of wound infections.

Check Digit Verification of cas no

The CAS Registry Mumber 4706-81-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,7,0 and 6 respectively; the second part has 2 digits, 8 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 4706-81:
(6*4)+(5*7)+(4*0)+(3*6)+(2*8)+(1*1)=94
94 % 10 = 4
So 4706-81-4 is a valid CAS Registry Number.
InChI:InChI=1/C14H30O/c1-3-4-5-6-7-8-9-10-11-12-13-14(2)15/h14-15H,3-13H2,1-2H3

4706-81-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name tetradecan-2-ol

1.2 Other means of identification

Product number -
Other names 2-TETRADECANOL

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:4706-81-4 SDS

4706-81-4Relevant articles and documents

Cleavage of tert-butyldimethylsilyl ethers by chloride ion

Farras, Jaume,Serra, Carme,Vilarrasa, Jaume

, p. 327 - 330 (2007/10/03)

A general method for the selective cleavage of tert-butyldimethylsilyl ethers in the presence of tert-butyldiphenylsilyl ones has been established using a combination of H2O and a concentrated solution of LiCl in DMF at 90°C. Since no acids, bases, reducing or oxidizing agents are used, the method seems to be very appropiate for the deprotection of TBDMS ethers in the presence of other sensitive functional groups.

A refined method for the removal of the methoxymethyl (MOM) protecting group for carbinols with acidic ion-exchange resin

Seto,Mander

, p. 2823 - 2828 (2007/10/02)

The methoxymethyl protecting group for carbinols is best removed from acid-sensitive substrates by hydrolysis in aqueous methanol using a cationic exchange resin (Dowex-50W).

Rates and Alkyl Group Size in Solvolysis of Alkyl Derivatives

Orlovic, Mirko,Kronja, Olga,Humski, Kresimir,Borcic, Stanko,Polla, Eugenio

, p. 3253 - 3256 (2007/10/02)

The logarithm of solvolysis rate constants in 80percent aqueous ethanol of 1,1-dimethyl-1-alkyl chlorides 1 and 1-phenyl-1-alkyl chlorides 2 decrease monotonically with increasing number of carbon atoms in the alkyl group.The first member of both series deviates from the corresponding correlation lines which have the some slope.In contrast, solvolysis rates in 80percent aqueous ethanol of 1-methyl-1-alkyl tosylates 3 do not depend upon the size of the alkyl group.The results are rationalized in terms of a mechanism that is very similar in reactions of series 1 and 2 but different from that of series 3.

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 4706-81-4