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24793-83-7

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24793-83-7 Usage

Description

1-(4-methoxyphenyl)-2,2-dimethylpropane-1,3-diol, also known as Bisabolol, is a chemical compound derived from the essential oil of chamomile. It is recognized for its anti-inflammatory, anti-irritant, and anti-microbial properties, which contribute to its wide range of applications across various industries.

Uses

Used in Cosmetic and Personal Care Industry:
1-(4-methoxyphenyl)-2,2-dimethylpropane-1,3-diol is used as an active ingredient for its soothing and skin-healing properties, making it ideal for products targeting sensitive or irritated skin.
Used in Pharmaceutical Industry:
In the pharmaceutical sector, 1-(4-methoxyphenyl)-2,2-dimethylpropane-1,3-diol is utilized as an anti-inflammatory agent, contributing to the effectiveness of medical ointments and related products.
Used in Fragrance Industry:
1-(4-methoxyphenyl)-2,2-dimethylpropane-1,3-diol is employed as a fragrance component for its pleasant, floral scent, enhancing the sensory experience of various products.
Overall, Bisabolol's safety and non-irritating nature render it a versatile compound suitable for a broad spectrum of applications in the cosmetic, pharmaceutical, and fragrance industries.

Check Digit Verification of cas no

The CAS Registry Mumber 24793-83-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,4,7,9 and 3 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 24793-83:
(7*2)+(6*4)+(5*7)+(4*9)+(3*3)+(2*8)+(1*3)=137
137 % 10 = 7
So 24793-83-7 is a valid CAS Registry Number.

24793-83-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(4-methoxyphenyl)-2,2-dimethylpropane-1,3-diol

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:24793-83-7 SDS

24793-83-7Relevant articles and documents

Heterocyclization involving benzylic C(sp3)-H functionalization enabled by visible light photoredox catalysis

Pandey, Ganesh,Laha, Ramkrishna,Mondal, Pradip Kumar

supporting information, p. 9689 - 9692 (2019/08/15)

A general and efficient method for heterocyclization involving benzylic C(sp3)-H functionalization enabled by visible light photoredox catalysis to access a wide range of structurally diverse oxygen as well as nitrogen heterocycles up to a gram scale is reported. The potential application of this new methodology is demonstrated by the total synthesis of (-)-codonopsinine and (+)-centrolobine. Herein it is proposed that selectfluor, unlike a fluorinating reagent, acts as an oxidative quencher and a hydrogen radical acceptor.

Synthesis and biological activity of cis 2-(6-chloropyridine-3-yl) methylamino-4-substitutedphenyl-5,5-dimethyl-1,3,2-dioxaphosphinane 2-oxides

De, Qing Shi,Liu, Yi,Feras,Xiao, Song Tan,Jian, Xin Chen

, p. 1937 - 1946 (2007/10/03)

A series of novel, asymmetric-cyclic phosphoramides containing substituted pyridine were synthesized via the condensation reactions of trans 2-chloro-4-substitutedphenyl-5, 5-dimethyl-1,3,2-dioxaphosphinane 2-oxide with 2-chloro-5-aminomethylpyridine or 3

Fluoride-induced chemiluminescent decomposition of dioxetanes bearing a siloxyaryl moiety to produce an alkyl aryl ketone as an emitter

Watanabe, Nobuko,Nagashima, Yasuhiro,Yamazaki, Takahiro,Matsumoto, Masakatsu

, p. 4811 - 4819 (2007/10/03)

Tetrabutylammonium fluoride induces the decomposition of 1-tert-butyl-4,4-dimethyl-5-(3-siloxyphenyl)-2,6,7-trioxabicyclo[3.2.0] heptane (4a) in DMSO to form an oxyanion of aromatic ketone (14a) as an emitter with high singlet-chemiexcitation yield comparable with that for a chemically initiated electron exchange luminescence (CIEEL) active dioxetane producing an oxyanion of aromatic ester as an emitter. A 7-siloxynaphthalen-2-yl analog (4b) was found on similar treatment to emit light with the maximum wavelength the longest among CIEEL-active dioxetanes hitherto known.

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