)-2-Acetoxypropionyl chloride
(S)-(−)-2-Acetoxypropionyl chloride
CAS: 36394-75-9
Molecular Formula: C5H7ClO3
)-2-Acetoxypropionyl chloride - Names and Identifiers
| Name | (S)-(− )-2-Acetoxypropionyl chloride |
| Synonyms | AP-CL 36394-75-9 O-ACETYL-L-LACTYL CHLORIDE S-ACETOXYPROPIONYL CHLORIDE 2-Acetoxy propionyl chloride )-2-Acetoxypropionyl chloride (S)-2-ACETOXYPROPIONYL CHLORIDE (S)-(-)-O-ACETYLLACTOYL CHLORIDE (S)-(-)-2-ACETOXYPROPIONYL CHLORIDE (1S)-2-chloro-1-methyl-2-oxoethyl acetate (1R)-2-chloro-2-oxo-1-phenylethyl acetate acetic acid (1-chloro-1-oxopropan-2-yl) ester |
| CAS | 36394-75-9 |
| EINECS | 420-610-4 |
| InChI | InChI=1/C5H7ClO3/c1-3(5(6)8)9-4(2)7/h3H,1-2H3/t3-/m0/s1 |
)-2-Acetoxypropionyl chloride - Physico-chemical Properties
| Molecular Formula | C5H7ClO3 |
| Molar Mass | 150.56 |
| Density | 1.189g/mLat 25°C(lit.) |
| Boling Point | 50°C5mm Hg(lit.) |
| Specific Rotation(α) | -31o (C=4 IN CHLOROFORM) |
| Flash Point | >230°F |
| Vapor Presure | 2.022mmHg at 25°C |
| Appearance | clear liquid |
| Specific Gravity | 1.19 |
| Color | Colorless to Light yellow |
| BRN | 1722943 |
| Storage Condition | Inert atmosphere,2-8°C |
| Refractive Index | n20/D 1.423(lit.) |
| MDL | MFCD00145252 |
)-2-Acetoxypropionyl chloride - Risk and Safety
| Hazard Symbols | C - Corrosive |
| Risk Codes | R34 - Causes burns R43 - May cause sensitization by skin contact R22 - Harmful if swallowed |
| Safety Description | S26 - In case of contact with eyes, rinse immediately with plenty of water and seek medical advice. S36/37/39 - Wear suitable protective clothing, gloves and eye/face protection. S45 - In case of accident or if you feel unwell, seek medical advice immediately (show the label whenever possible.) S23 - Do not breathe vapour. |
| UN IDs | UN 3265 8/PG 2 |
| WGK Germany | 3 |
| FLUKA BRAND F CODES | 10-21 |
| Hazard Class | 8 |
| Packing Group | III |
)-2-Acetoxypropionyl chloride - Reference Information
| Use | Commonly used chiral structural units. It is also used to decompose bicyclic α-hydroxy lactones and to prepare chiral phosphonates for enantiomeric excess detection of unprotected amino acids. Effective chiral derivatization agent. Effective chiral derivative. |
Last Update：2024-04-10 22:29:15
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