Welcome to LookChem.com Sign In|Join Free
  • or
3-[4-(1,1-dimethylethyl)phenyl]propenyl acetate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

77104-99-5

Post Buying Request

77104-99-5 Suppliers

Recommended suppliers

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

77104-99-5 Usage

General Description

3-[4-(1,1-dimethylethyl)phenyl]propenyl acetate, also known as benzyl t-butyl vinyl ether, is a chemical compound with the molecular formula C15H20O2. It is an aromatic compound and a member of the class of acetates that is derived from acetic acid. This chemical is commonly used in fragrances, flavors, and cosmetics due to its pleasant odor and ease of blending with other compounds. It is a colorless liquid with a fruity, floral, and slightly woody odor. Additionally, it is used as an intermediate for the synthesis of pharmaceuticals and other organic compounds. Studies have shown that it has low toxicity and is not expected to have any harmful effects on human health when used in appropriate quantities.

Check Digit Verification of cas no

The CAS Registry Mumber 77104-99-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,7,1,0 and 4 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 77104-99:
(7*7)+(6*7)+(5*1)+(4*0)+(3*4)+(2*9)+(1*9)=135
135 % 10 = 5
So 77104-99-5 is a valid CAS Registry Number.
InChI:InChI=1/C15H20O2/c1-12(16)17-11-5-6-13-7-9-14(10-8-13)15(2,3)4/h5,7-11H,6H2,1-4H3/b11-5+

77104-99-5SDS

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 3-(4-(tert-butyl)phenyl)prop-1-en-1-yl acetate

1.2 Other means of identification

Product number -
Other names 3-[4-(1,1-DIMETHYLETHYL)PHENYL]PROPENYL ACETATE

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:77104-99-5 SDS

77104-99-5Downstream Products

77104-99-5Relevant academic research and scientific papers

Synthesis method of tert-butyl phenylpropionaldehyde

-

Paragraph 0010; 0037; 0039; 0041; 0043; 0045; 0047, (2021/03/30)

The invention discloses a synthesis method of tert-butyl phenylpropionaldehyde and relates to the field of perfume raw material synthesis, the method comprises the following steps: 1) synthesis of allylidene di(acetate)(AEDA): acetic anhydride and acrolein react at a certain temperature under the action of a catalyst A to obtain AEDA, 2) synthesis of a bourgeonal(BGA) precursor: tert-butylbenzeneand AEDA react at a certain temperature under the action of a catalyst B to obtain ortho-position and para-position BGA precursors, and 3) alcoholysis on the BGA precursor to prepare the BGA: the BGAprecursor, a solvent and a catalyst C react at a certain temperature to obtain the ortho-BGA and the para-BGA. Tert-butylbenzene is used as an initial raw material, acrolein is subjected to aldehyde group protection by acetic anhydride, then condensation is performed to obtain precursors of ortho-position and para-position bordeaux aldehyde, and an ortho-position and para-position tert-butylphenylpropionaldehyde mixed product is obtained through aldehyde group protection removal by hydrolysis, and the method is simple in process, low in raw material price, less in three wastes and elegant in fragrance, and can realize mass production.

CATALYTIC SCRIABINE REACTION

-

Page/Page column 5, (2008/06/13)

The present invention relates to the field of organic synthesis. More particularly it provides a process for making aromatic non-conjugated enol esters or enol ethers from an aromatic compound or moiety and a protected enal compound or moiety, such as an acetal or an acylal. The reaction is promoted by a salt of formula MX1-4, M representing a transition metal such as Zn or Fe and X representing a mono-anion, or by BY3, wherein Y represents a fluoride or a phenyl group optionally substituted.

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 Customer Service

What can I do for you?
Get Best Price

Get Best Price for 77104-99-5