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Benzenemethanol, 2-hydroxy-5-methoxy-α-(2-methyl-1-propenyl)-, also known as vanillyl alcohol, is a naturally occurring organic compound with the chemical formula C10H14O3. It is a derivative of benzyl alcohol, featuring a hydroxyl group at the 2-position, a methoxy group at the 5-position, and a 2-methyl-1-propenyl group at the α-position. Benzenemethanol, 2-hydroxy-5-methoxy-a-(2-methyl-1-propenyl)- is found in various plants and is known for its antioxidant, anti-inflammatory, and analgesic properties. It is also used as a flavoring agent and fragrance component in the food and cosmetics industries. Vanillyl alcohol is a key intermediate in the synthesis of vanillin, the primary component responsible for the characteristic aroma and taste of vanilla.

88252-66-8

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88252-66-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 88252-66-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,8,2,5 and 2 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 88252-66:
(7*8)+(6*8)+(5*2)+(4*5)+(3*2)+(2*6)+(1*6)=158
158 % 10 = 8
So 88252-66-8 is a valid CAS Registry Number.

88252-66-8SDS

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 2-(1-Hydroxy-3-methyl-but-2-enyl)-4-methoxy-phenol

1.2 Other means of identification

Product number -
Other names -

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

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Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:88252-66-8 SDS

88252-66-8Relevant academic research and scientific papers

A catalytic approach for the synthesis of allylic azides from aryl vinyl carbinols

Srinu,Srihari

supporting information, p. 2382 - 2385 (2013/06/27)

A metal-free and catalytic approach for the preparation of allylic azides starting from aryl vinyl carbinols is described herein.

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