Ethyl α-Iodophenylacetate
Product Information
Molecular Formula
C10H11IO2
Molecular Weight
290.10
Description
P501 P210 P264 P280 P302 + P352 P370 + P378 P337 + P313 P305 + P351 + P338 P362+P364 P332 + P313 P403 + P235
Synonyms
Ethyl alpha-Iodophenylacetate; alpha-Iodophenylacetic acid ethyl ester; Benzeneacetic acid, α-iodo-, ethyl ester; 2-Iodo-2-phenylacetic acid ethyl ester
IUPAC Name
ethyl 2-iodo-2-phenylacetate
SMILES
CCOC(=O)C(C1=CC=CC=C1)I
InChI
InChI=1S/C10H11IO2/c1-2-13-10(12)9(11)8-6-4-3-5-7-8/h3-7,9H,2H2,1H3
InChI Key
GFYUBPKXVMWINH-UHFFFAOYSA-N
Boiling Point
302.2±30.0 °C at 760 mmHg
Flash Point
137 °C
Purity
≥97%
Density
1.626±0.06 g/cm3
Appearance
Light yellow to Brown clear liquid
Storage
Store at -20 °C
Refractive Index
1.58
Safety Information
Hazards
H314 H290
Precautionary Statement
P501 P234 P264 P280 P390 P303 + P361 + P353 P301 + P330 + P331 P363 P304 + P340 + P310 P305 + P351 + P338 + P310 P406 P405
Computed Properties
XLogP3
2.9
Hydrogen Bond Donor Count
0
Hydrogen Bond Acceptor Count
2
Rotatable Bond Count
4
Exact Mass
289.98038 g/mol
Monoisotopic Mass
289.98038 g/mol
Topological Polar Surface Area
26.3Ų
Heavy Atom Count
13
Formal Charge
0
Complexity
164
Isotope Atom Count
0
Defined Atom Stereocenter Count
0
Undefined Atom Stereocenter Count
1
Defined Bond Stereocenter Count
0
Undefined Bond Stereocenter Count
0
Covalently-Bonded Unit Count
1
Compound Is Canonicalized
Yes
Patents
| Publication Number | Title | Priority Date |
|---|---|---|
| CN-113388058-A | Method for full-spectrum induced controllable free radical polymerization by using organic catalyst | 2021-06-08 |
| CN-112724345-A | Conjugated microporous polymer, preparation method thereof and application thereof in visible light induced controllable free radical polymerization | 2020-12-23 |
| CN-112724345-B | Conjugated microporous polymer, preparation method thereof and application thereof in visible light induced controllable free radical polymerization | 2020-12-23 |
| CN-111909322-A | Synthesis of graft copolymer by combining near infrared light induced iodine regulation RDRP and ultraviolet light induced ring-opening polymerization one-pot method | 2020-07-29 |
| CN-111909322-B | Synthesis of graft copolymer by combining near infrared light induced iodine regulation RDRP and ultraviolet light induced ring-opening polymerization one-pot method | 2020-07-29 |
| CN-111440279-A | Preparation method of block polymer with adjustable molecular weight distribution | 2020-05-26 |
| WO-2021215380-A1 | Carboxyl group-containing crosslinked polymer or salt thereof, and use thereof | 2020-04-23 |
| WO-2021215381-A1 | Method for producing carboxyl group-containing crosslinked polymer or salt thereof | 2020-04-23 |
| JP-2021100996-A | Block copolymers, resin compositions and adhesive films | 2019-12-24 |
| JP-2021095440-A | Resin compositions, stretchable conductors, electronic devices and adhesive films | 2019-12-13 |
Literatures
| PMID | Publication Date | Title | Journal |
|---|---|---|---|
| 4926 | 1976-01-01 | [Proceedings: The clinical importance and mechanism of changes in gamma-glutamyl transpeptidase in liver diseases] | Vutreshni bolesti |
