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18448-88-9

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18448-88-9 Usage

Chemical Class

Phenols

Occurrence

Essential oils of plants like basil, bay leaf, and cinnamon

Aroma

Spicy, sweet, and clove-like

Usage

Popular ingredient in fragrance and flavor industries

Potential Properties

Antimicrobial and antioxidant

Precaution

Can cause skin and eye irritation, handle with care.

Check Digit Verification of cas no

The CAS Registry Mumber 18448-88-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,8,4,4 and 8 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 18448-88:
(7*1)+(6*8)+(5*4)+(4*4)+(3*8)+(2*8)+(1*8)=139
139 % 10 = 9
So 18448-88-9 is a valid CAS Registry Number.
InChI:InChI=1/C10H12O/c1-2-3-6-9-7-4-5-8-10(9)11/h2-5,7-8,11H,6H2,1H3/b3-2+

18448-88-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-but-2-enylphenol

1.2 Other means of identification

Product number -
Other names 2-Crotyl-phenol

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:18448-88-9 SDS

18448-88-9Relevant articles and documents

Identification of a boron-containing intermediate in the boron tribromide mediated aryl propargyl ether cleavage reaction

Yao, Min-Liang,Reddy, Marepally Srinivasa,Zeng, Wenbin,Hall, Kelly,Walflsh, Ingrid,Kabalka, George W.

supporting information; experimental part, p. 1385 - 1387 (2009/07/04)

An alternate reaction mechanism for the boron tribromide mediated deprotection of aryl propargyl ethers based on the isolation of a key boron-containing byproduct is proposed. On the basis of the new mechanistic insight, we discovered that HBBr2 · SMe2 can also be used for cleaving aryl propargyl ethers.

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