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4-tert-butyl-2-Methoxybenzaldehyde is a chemical compound with the molecular formula C12H16O2. It is a white to light yellow crystalline powder known for its sweet, floral, and fruity odor.

53535-88-9

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53535-88-9 Usage

Uses

Used in Food Industry:
4-tert-butyl-2-Methoxybenzaldehyde is used as a flavoring agent for its distinctive sweet, floral, and fruity aroma, enhancing the taste and smell of various food products.
Used in Perfumes and Cosmetics:
In the perfumery and cosmetics industry, 4-tert-butyl-2-Methoxybenzaldehyde serves as a fragrance ingredient, adding a pleasant and long-lasting scent to products such as perfumes, colognes, and body care items.
Used in Pharmaceutical Industry:
4-tert-butyl-2-Methoxybenzaldehyde is utilized as an intermediate in the synthesis of various drugs, contributing to the development of new medications.
Used in Antioxidant and Antimicrobial Applications:
Due to its antioxidant and antimicrobial properties, 4-tert-butyl-2-Methoxybenzaldehyde is a valuable ingredient in the formulation of pharmaceutical and cosmetic products, promoting health and hygiene.

Check Digit Verification of cas no

The CAS Registry Mumber 53535-88-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,3,5,3 and 5 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 53535-88:
(7*5)+(6*3)+(5*5)+(4*3)+(3*5)+(2*8)+(1*8)=129
129 % 10 = 9
So 53535-88-9 is a valid CAS Registry Number.

53535-88-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-Methoxy-4-(2-methyl-2-propanyl)benzaldehyde

1.2 Other means of identification

Product number -
Other names 4-t-Butylnitrobenzene

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:53535-88-9 SDS

53535-88-9Downstream Products

53535-88-9Relevant academic research and scientific papers

Synthesis of novel structurally simplified estrogen analogues with electron-donating groups in ring A

Tietze, Lutz F.,Vock, Carsten A.,Krimmelbein, Ilga K.,Nacke, Linda

experimental part, p. 2040 - 2060 (2009/12/27)

A library of 25 novel estrogen analogues were prepared in five to eight steps from mostly commercially available substituted anisoles via bromination, formylation, Corey-Fuchs reaction, elimination, and Sonogashira reaction. Georg Thieme Verlag Stuttgart.

Selective preparation of polycyclic aromatic hydrocarbons. Part 4. New synthetic route to anthracenes from diphenylmethanes using Friedel-Crafts intramolecular cyclization

Yamato, Takehiko,Sakaue, Naozumi,Shinoda, Naoki,Matsuo, Koji

, p. 1193 - 1199 (2007/10/03)

Preparation of several anthracenes from diphenylmethanes by direct Bradsher-type reaction, which incorporates formylation of a hydrocarbon followed by Friedel-Crafts intramolecular cyclization, is presented. The present method involving the action of Cls

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