1-Ethynyl-4-iodoben­zene CAS 766-99-4

• Iden­ti­fi­ca­tion
• Prop­er­ties
• Safe­ty Data
• Spec­i­fi­ca­tions & Oth­er Information
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Iden­ti­fi­ca­tion

CAS Number

766-99-4

Name

1-Ethynyl-4-iodoben­zene

Syn­onyms

1-Ethinyl-4-iod­ben­­zol

[Ger­man]

[IUPAC name – gen­er­at­ed by ACD/​Name]
1-Ethynyl-4-iodoben­zene

[IUPAC name – gen­er­at­ed by ACD/​Name]
1-Éthynyl-4-iodoben­zène

[French]

[IUPAC name – gen­er­at­ed by ACD/​Name]
766-99-4

[RN]
Ben­zene, 1-ethynyl-4-iodo-

[IUPAC index name – gen­er­at­ed by ACD/​Name]

SMILES

C#Cc1ccc(I)cc1

Std­InChI

InChI=1S/C8H5I/c1-2-7-3-5-8(9)6-4-7/h1,3-6H

Std­InChIKey

MYGX­ITK­L­GQBZBV-UHF­F­­FAOYSA-N

Mol­e­c­u­lar Formula

C8H5I

Mol­e­c­u­lar Weight

228.032

Prop­er­ties

Appear­ance

Yel­low liquid

Safe­ty Data

Sym­bol

GHS07

Sig­nal Word

Warn­ing

Haz­ard statements

Pre­cau­tion­ary Statements

WGK Germany

3

MSDS Download

Spec­i­fi­ca­tions and Oth­er Infor­ma­tion of Our 1-Ethynyl-4-iodoben­zene CAS 766-99-4

Iden­ti­fi­ca­tion Methods

HPLC

Puri­ty

97% min

Known Appli­ca­tion

1. Cross-Cou­­pling Reac­tions : Wide­ly used in Sono­gashira cou­pling, Suzu­ki cou­pling, and oth­er pal­la­di­um-cat­­a­lyzed reac­tions to con­struct aryl – alkynyl or aryl – aryl bonds. 2. Phar­ma­ceu­ti­cal Inter­me­di­ates : Serves as a build­ing block for the syn­the­sis of bioac­tive mol­e­cules and drug can­di­dates con­tain­ing alkynyl-aryl struc­tures. 3. Mate­r­i­al Sci­ence : Used in the prepa­ra­tion of func­tion­al poly­mers, con­ju­gat­ed mate­ri­als, and opto­elec­tron­ic com­pounds due to its alkyne func­tion­al­i­ty. 4. Het­e­ro­cyclic Syn­the­sis : Acts as a pre­cur­sor for the con­struc­tion of het­eroaryl deriv­a­tives, which are valu­able in agro­chem­i­cals and pharmaceuticals.

Gen­er­al View of Documents

Links

This prod­uct is devel­oped by our R&D com­pa­ny Cam­ing Phar­ma­ceu­ti­cal Lim­it­ed (http://​www​.cam​ing​.com/).

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