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1224157-88-3

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1224157-88-3 Usage

General Description

Tert-butyl 3-formyl-4-hydroxybenzoate is a chemical compound with a molecular formula C13H16O4. It is a derivative of benzoic acid and is commonly used as a building block in organic synthesis. The tert-butyl group on the molecule provides steric hindrance, which can affect its reactivity and stability. The 3-formyl and 4-hydroxy groups make it a potential precursor for pharmaceuticals and agrochemicals. It is a white to off-white crystalline solid, and its properties make it suitable for use in various industries, including pharmaceuticals, cosmetics, and fragrances. tert-Butyl 3-formyl-4-hydroxybenzoate has potential applications in the development of new drugs or as a component in other chemical reactions.

Check Digit Verification of cas no

The CAS Registry Mumber 1224157-88-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,2,4,1,5 and 7 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1224157-88:
(9*1)+(8*2)+(7*2)+(6*4)+(5*1)+(4*5)+(3*7)+(2*8)+(1*8)=133
133 % 10 = 3
So 1224157-88-3 is a valid CAS Registry Number.

1224157-88-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-Methyl-2-propanyl 3-formyl-4-hydroxybenzoate

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

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

More Details:1224157-88-3 SDS

1224157-88-3Downstream Products

1224157-88-3Relevant articles and documents

Oxidative dearomatization: Synthesis of functionalized bicyclo[2.2.2]octenones, sigmatropic shift in excited state, and radical-induced cleavage of cyclopropane ring

Arora, Karan,Singh, Vishwakarma

, p. 3552 - 3562 (2014)

Synthesis of novel bicyclo[2.2.2]octenones endowed with a β,γ-enone system in which γ-carbon is substituted with an electron-withdrawing group from simple aromatics is described. Oxa-di-pi-methane reaction of bicyclo[2.2.2]octenones to functionalized bicy

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