- 2'-Chloroacetophenone
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2026-07-06
- CAS:2142-68-9
- Min. Order: 1KG
- Purity: 98%min
- Supply Ability: 30tons/month
- 2'-Chloroacetophenone
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- $10.00
-
2026-05-28
- CAS:2142-68-9
- Min. Order: 1KG
- Purity: 99.%
- Supply Ability: 10 ton
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| | 2'-Chloroacetophenone Basic information |
| | 2'-Chloroacetophenone Chemical Properties |
| Melting point | 52-56C | | Boiling point | 227-230 °C | | density | 1.190 g/mL at 20 °C | | refractive index | n20/D 1.544 | | Fp | 192 °F | | storage temp. | Store below +30°C. | | solubility | Chloroform, DMSO (Slightly), Methanol (Slightly) | | form | Liquid | | Specific Gravity | 1.19 | | color | Clear light yellow to amber | | Sensitive | Lachrymatory | | BRN | 1858916 | | InChI | 1S/C8H7ClO/c1-6(10)7-4-2-3-5-8(7)9/h2-5H,1H3 | | InChIKey | ZDOYHCIRUPHUHN-UHFFFAOYSA-N | | SMILES | CC(=O)c1ccccc1Cl | | CAS DataBase Reference | 2142-68-9(CAS DataBase Reference) | | NIST Chemistry Reference | Ethanone, 1-(2-chlorophenyl)-(2142-68-9) | | EPA Substance Registry System | Ethanone, 1-(2-chlorophenyl)- (2142-68-9) |
| Hazard Codes | Xn,Xi,T+ | | Risk Statements | 22-36/37-36/37/38-26 | | Safety Statements | 26-36-37/39-45-36/37/39-28A | | RIDADR | UN 3416 6.1/PG 2 | | WGK Germany | 3 | | RTECS | AM6310000 | | Hazard Note | Harmful/Irritant/Lachrymatory | | TSCA | TSCA listed | | HazardClass | 6.1 | | PackingGroup | II | | HS Code | 29147090 | | Storage Class | 6.1A - Combustible acute toxic Cat. 1 and 2
very toxic hazardous materials | | Hazard Classifications | Acute Tox. 4 Oral
Eye Irrit. 2
Skin Irrit. 2
STOT SE 3 | | Toxicity | LD50 orally in Rabbit: 1820 mg/kg |
| | 2'-Chloroacetophenone Usage And Synthesis |
| Chemical Properties | clear light yellow to amber liquid | | Uses | 2''-Chloroacetophenone (cas# 2142-68-9) is a compound useful in organic synthesis. | | Uses | 2′-Chloroacetophenone was employed as model substrate to investigate the enzymatic performance of Aspergillus terreus and Rhizopus oryzae in enantioselective bioreductions using glycerol as a co-solvent. | | General Description | 2′-Chloroacetophenone undergoes stereoselective reduction to (R)-2′-chloro-1-phenyl-ethanol by Saccharomyces cerevisiae B5. It is commonly used as lacrimator. |
| | 2'-Chloroacetophenone Preparation Products And Raw materials |
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