Name | N-Chloromethylphthalimide |
Synonyms | AKOS BBS-00000871 TIMTEC-BB SBB000346 Chloromethylphthalimide N-Chloromethylphthalimide N-(Chloromethyl)phthalimide N-(CHLOROMETHYL)PHTHALIMIDE N-Chloromethyltrimellitimide 2-(chloromethyl)-1h-isoindole-3(2h)-dione 2-(CHLOROMETHYL)-1H-ISOINDOLE-1,3(2H)-DIONE 1H-Isoindole-1,3(2H)-dione, 2-(chloromethyl)- |
CAS | 17564-64-6 |
EINECS | 241-541-4 |
InChI | InChI=1/C9H6ClNO2/c10-5-11-8(12)6-3-1-2-4-7(6)9(11)13/h1-4H,5H2 |
Molecular Formula | C9H6ClNO2 |
Molar Mass | 195.6 |
Density | 1.3228 (rough estimate) |
Melting Point | 131-135 °C (lit.) |
Boling Point | 305.2±25.0 °C(Predicted) |
Water Solubility | slightly soluble |
Solubility | chloroform: soluble50mg/mL |
Appearance | White powder |
Color | White to Almost white |
BRN | 140942 |
pKa | -2.63±0.20(Predicted) |
Storage Condition | 2-8°C |
Sensitive | Easily absorbing moisture |
Refractive Index | 1.5790 (estimate) |
MDL | MFCD00005898 |
Physical and Chemical Properties | White crystalline powder |
Use | It was used in the synthesis of aminomethyl copoly-(styrene-l%-divinylbenzene) resins of high purity, in esterification of 12S-hydroxylabda-8(17),13(16),14-trien-19-oic acid, new labdane-type diterpenoid, in esterification of 13-ethoxylabda-8(17),11 |
Risk Codes | R36/37/38 - Irritating to eyes, respiratory system and skin. R52/53 - Harmful to aquatic organisms, may cause long-term adverse effects in the aquatic environment. 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 - Wear suitable protective clothing. S37/39 - Wear suitable gloves and eye/face protection S61 - Avoid release to the environment. Refer to special instructions / safety data sheets. S45 - In case of accident or if you feel unwell, seek medical advice immediately (show the label whenever possible.) |
UN IDs | UN 2811 6.1 / PGIII |
WGK Germany | 3 |
FLUKA BRAND F CODES | 9-21 |
TSCA | Yes |
HS Code | 29251995 |
NIST chemical information | Information provided by: webbook.nist.gov (external link) |
EPA chemical information | Information provided by: ofmpub.epa.gov (external link) |
uses | pesticide intermediates. |
Production method | Phthalimide is obtained by reacting phthalic anhydride with ammonium bicarbonate, and then hydroxylation and chlorination. 1. Preparation of o-dimethyl imide The phthalic anhydride and ammonium bicarbonate are reacted to obtain phthalimide. 2. Preparation of N-hydroxymethylbenzodiimide The reaction of formaldehyde with phthalimide produces N-hydroxymethylbenzodiimide. 3. Preparation of chloromethylbenzimide N-chloromethylbenzimide was prepared from N-hydroxymethylbenzimide. |