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CAS

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21375-88-2

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21375-88-2 Usage

Appearance

White to light yellow crystalline solid

Usage

Synthesis of organic compounds and pharmaceuticals

Chemical Groups

Bromine atom, phenyl group, ethynyl group

Versatility

Building block for creating complex molecules

Potential Applications

Materials science, precursor in chemical reactions

Safety Precautions

Potential irritant, hazardous effects if not properly handled or used

Check Digit Verification of cas no

The CAS Registry Mumber 21375-88-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,1,3,7 and 5 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 21375-88:
(7*2)+(6*1)+(5*3)+(4*7)+(3*5)+(2*8)+(1*8)=102
102 % 10 = 2
So 21375-88-2 is a valid CAS Registry Number.

21375-88-2Relevant articles and documents

Incorporation of Palladium Catalyst Inside Cross-Linked Chitosan Hybrid Nanofibers for the Sonogashira Reaction

Zhong, S.

, p. 480 - 485 (2020)

Abstract: Nanofibers are attractive supporting matrices for catalytically active metallic catalysts. Herein, palladium species were successfully incorporated into the modified chitosan/poly(ethylene oxide)/maleic acid nanofibers by electrospinning. Then,

Diaryl acetylene compound containing methylene quinone as well as preparation method and application of diaryl acetylene compound

-

Paragraph 0011; 0017; 0040-0042; 0061-0063, (2021/06/09)

The invention discloses a diaryl acetylene compound containing methylene quinone as well as a preparation method and application thereof, and belongs to the technical field of pharmacy and chemical industry. The structural formula of the diarylacetylene c

Gold-Catalyzed Cascade and Divergent Synthesis of Indolobenzazepines and Indoloquinolines from Nitrogen-Tethered 1,8-Diynes

Ito, Mamoru,Onoda, Hideaki,Shibata, Takanori,Takaki, Asahi

supporting information, (2022/01/22)

We describe the divergent construction of two nitrogen-containing polycyclic systems by gold-catalyzed cycloisomerizations. The gold-catalyzed cascade hydroamination and 7-endo-dig-selective cycloisomerization of nitrogen-tethered 1,8-diynes yielded indol

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