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405-29-8

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405-29-8 Usage

Physical State

Colorless liquid

Odor

Strong aromatic

Usage

Pharmaceutical and chemical industries

Classification

Fluorobenzene derivative

Functional Groups

Contains a fluorine and a phenylethynyl group

Application

Building block in the synthesis of pharmaceuticals and agrochemicals

Reactivity

Unique chemical reactivity

Biological Activity

Potential biological activity

Additional Uses

Production of dyes, pigments, and specialty chemicals

Safety

Proper handling and storage procedures required

Check Digit Verification of cas no

The CAS Registry Mumber 405-29-8 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 4,0 and 5 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 405-29:
(5*4)+(4*0)+(3*5)+(2*2)+(1*9)=48
48 % 10 = 8
So 405-29-8 is a valid CAS Registry Number.

405-29-8SDS

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-fluoro-4-(2-phenylethynyl)benzene

1.2 Other means of identification

Product number -
Other names 1-FLUORO-4-PHENYLETHYNYL-BENZENE

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:405-29-8 SDS

405-29-8Relevant articles and documents

Diamondoid phosphines - Selective phosphorylation of nanodiamonds

Schwertfeger, Hartmut,Machuy, Mareike M.,Wuertele, Christian,Dahl, Jeremy E. P.,Carlson, Robert M. K.,Schreiner, Peter R.

, p. 609 - 615 (2010)

The diamondoids (nanodiamonds) diamantarle and triamantane were selectively converted into diorganophosphinic acid chlorides by reacting them with phosphorus trichloride under Friedel-Crafts-like conditions. The di-diamondoid phosphinic acid chlorides wer

Lipids as versatile solvents for chemical synthesis

Bayer, Annette,Gevorgyan, Ashot,Hopmann, Kathrin H.

supporting information, p. 7219 - 7227 (2021/09/28)

Development of safe, renewable, cheap and versatile solvents is a longstanding challenge in chemistry. We show here that vegetable oils and related systems can become prominent solvents for organic synthesis. Suzuki-Miyaura, Hiyama, Stille, Sonogashira and Heck cross-couplings proceed with quantitative yields in a range of vegetable oils, fish oil, butter and waxes used as solvents. Appropriate methodologies for high-throughput screening and sustainable isolation techniques applicable for vegetable oils and related lipids are presented.

Simple and efficient diaryl alkyne synthesis method

-

Paragraph 0026; 0029-0031, (2021/04/14)

The embodiment of the invention discloses a simple and efficient diaryl alkyne synthesis method. The method comprises the steps of by taking arylmethylbenzotriazole and aromatic aldehyde as raw materials, carrying out addition and double-beta-elimination reaction under the action of bis (trimethylsilyl) amino salt MN (SiMe3) 2 to synthesize diaryl alkyne by a one-pot method. The raw materials and chemical reagents used in the method are easy to obtain, the reaction conditions are mild, the operation is simple, the substrate universality is good, the product yield is high, and the method is a simple and efficient diaryl alkyne synthesis method.

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