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15084-80-7 Usage

Physical state

Yellow liquid

Usage

a. Fragrance ingredient in perfumes and personal care products
b. Synthesis of pharmaceuticals and other organic compounds

Odor

Strong, sweet, and floral

Potential applications

a. Anti-inflammatory treatments
b. Anti-cancer treatments

Chemical structure

Contains a tert-butyl group attached to a phenyl ring, a sulfur atom, and a propanone group.

Check Digit Verification of cas no

The CAS Registry Mumber 15084-80-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,5,0,8 and 4 respectively; the second part has 2 digits, 8 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 15084-80:
(7*1)+(6*5)+(5*0)+(4*8)+(3*4)+(2*8)+(1*0)=97
97 % 10 = 7
So 15084-80-7 is a valid CAS Registry Number.

15084-80-7SDS

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	1-(4-tert-butylphenyl)sulfanylpropan-2-one

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:15084-80-7 SDS

15084-80-7Upstream product

15084-80-7Downstream Products

15084-80-7Relevant academic research and scientific papers

Synthesis of α-arylthioacetones using TEMPO as the: C 3 synthon via a reaction cascade of sequential oxidation, skeletal rearrangement and C-S bond formation

Zou, Jiao-Xia,Jiang, Yi,Lei, Shuai,Yin, Gao-Feng,Hu, Xiao-Ling,Zhao, Quan-Yi,Wang, Zhen

supporting information, p. 2341 - 2345 (2019/03/07)

Here, we present an unprecedented pathway to α-sulfenylated carbonyl compounds from commercially available thiols and universally employed TEMPO and its analogues, which act as C3 synthons through skeletal rearrangement under simple and metal-f

Synthesis and anticancer activity of new phenyl-ring substituted 4-morpholino-1-phenylthio-2-butanones [Mannich bases]

Siatra-Papastaikoudi,Tsotinis,Chinou,Roussakis

, p. 221 - 223 (2007/10/02)

The preparation of phenyl-ring substituted 4-morpholino-1-phenylthio-2-butanones 4a-e is described. These compounds were evaluated against P-388 leukemia and human cancer rhinopharynx KB cells in vitro; some compounds were found to exhibit activity agains

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15084-80-7

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