CIS-3-IODOACRYLIC ACID ETHYL ESTER

Product Name: CIS-3-IODOACRYLIC ACID ETHYL ESTER
CAS No.: 31930-36-6
Chemical Name: CIS-3-IODOACRYLIC ACID ETHYL ESTER
Synonyms: (Z)-ethyl 3-iodoacrylate;ETHYL CIS-3-IODOACRYLATE;ethyl (Z)-3-iodoacrylate;ethyl (Z)-3-iodopropenoate;Ethyl cis-3-iodoacrylate 98%;Ethyl cis-3-Iodoacrylate CIS-3-IODOACRYLIC ACID ETHYL ESTER;2-Propenoic acid, 3-iodo-, ethyl ester, (2Z)-;Ethylcis-3-Iodoacrylate(stabilizedwithCopperchip)>Ethyl cis-3-Iodoacrylate (stabilized with Copper chip)
CBNumber: CB1112593
Molecular Formula: C5H7IO2
Formula Weight: 226.01
MOL File: 31930-36-6.mol

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CIS-3-IODOACRYLIC ACID ETHYL ESTER Property

Boiling point:: 85 °C/20 mmHg (lit.)
Density: 1.765 g/mL at 25 °C (lit.)
refractive index: n20/D 1.533(lit.)
Flash point:: 210 °F
storage temp.: 2-8°C
solubility: Chloroform, Ethyl Acetate (Slightly)
form: Oil
color: Clear Colourless
CAS DataBase Reference: 31930-36-6

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Safety

Hazard Codes: Xi
Risk Statements: 36/37/38
Safety Statements: 26
WGK Germany: 3
HS Code: 29161900

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Hazard and Precautionary Statements (GHS)

Symbol(GHS)

Signal word

Warning

Hazard statements

H315Causes skin irritation

H319Causes serious eye irritation

H335May cause respiratory irritation

Precautionary statements

P261Avoid breathing dust/fume/gas/mist/vapours/spray.

P264Wash hands thoroughly after handling.

P264Wash skin thouroughly after handling.

P271Use only outdoors or in a well-ventilated area.

P280Wear protective gloves/protective clothing/eye protection/face protection.

P302+P352IF ON SKIN: wash with plenty of soap and water.

P305+P351+P338IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continuerinsing.

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N-Bromosuccinimide Price

Sigma-Aldrich

Product number: 423602
Product name: Ethyl cis-3-iodoacrylate
Purity: 98%
Packaging: 5g
Price: $174.6
Updated: 2024/03/01

Sigma-Aldrich

Product number: 423602
Product name: Ethyl cis-3-iodoacrylate
Purity: 98%
Packaging: 1g
Price: $59
Updated: 2023/06/20

TCI Chemical

Product number: I0502
Product name: Ethyl cis-3-Iodoacrylate (stabilized with Copper chip)
Purity: >98.0%(GC)
Packaging: 5g
Price: $208
Updated: 2024/03/01

TCI Chemical

Product number: I0502
Product name: Ethyl cis-3-Iodoacrylate (stabilized with Copper chip)
Purity: >98.0%(GC)
Packaging: 25g
Price: $604
Updated: 2024/03/01

TRC

Product number: E678625
Product name: Ethyl cis-3-iodoacrylate
Packaging: 2.5g
Price: $140
Updated: 2021/12/16

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CIS-3-IODOACRYLIC ACID ETHYL ESTER Chemical Properties,Usage,Production

Uses

Ethyl Cis-?3-?iodoacrylate is a reactant used in the synthesis of complex naphtho(benzo)furans as well as in the cobalt-catayzed cross coupling of functionalized organozinc pivalates.

Uses

Ethyl cis-3-iodoacrylate may be used in the synthesis of the following:

vinyl sulfides
(Z)-1-iodohept-1-en-3-ol
(E)-1-iodohept-1-en-3-ol
(Z)-β-iodoacrolein
6-oxo-M₁Guo

General Description

Ethyl cis-3-iodoacrylate (cis-ethyl-β-iodoacrylate, ethyl (Z)-β-iodoacrylate) is Z-vinyl iodide derivative. It is reported to be prepared from ethyl propiolate by treating with sodium iodide. Its Suzuki coupling reaction with cyclic vinyl boronic acids has been studied.

CIS-3-IODOACRYLIC ACID ETHYL ESTER Preparation Products And Raw materials

Raw materials

Preparation Products

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CIS-3-IODOACRYLIC ACID ETHYL ESTER Suppliers

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31930-36-6, CIS-3-IODOACRYLIC ACID ETHYL ESTERRelated Search:

ETHYL CIS-3-IODOCROTONATE, 97 (Z)-(3)-IODOACRYLIC ACID CIS-3-IODOACRYLIC ACID ETHYL ESTER

ethyl (Z)-3-iodoacrylate

ethyl (Z)-3-iodopropenoate

CIS-3-IODOACRYLIC ACID ETHYL ESTER

ETHYL CIS-3-IODOACRYLATE

Ethyl cis-3-Iodoacrylate (stabilized with Copper chip)

(Z)-ethyl 3-iodoacrylate

Ethyl cis-3-iodoacrylate 98%

Ethyl cis-3-Iodoacrylate&nbsp

Ethyl <i>cis</i>-3-Iodoacrylate (stabilized with Copper chip)

Ethylcis-3-Iodoacrylate(stabilizedwithCopperchip)&gt

2-Propenoic acid, 3-iodo-, ethyl ester, (2Z)-

31930-36-6

C5H7IO2

ICHCHCO2C2H5

Esters

Building Blocks

Carbonyl Compounds

C2 to C5

Organic Building Blocks

Building Blocks

C2 to C5

Carbonyl Compounds

Chemical Synthesis

Organic Building Blocks

C2 to C5

Carbonyl Compounds

Esters