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Home > Encyclopedia > 2-(Chloromethyl)-1H-isoindole-1,3(2H)-dione

2-(Chloromethyl)-1H-isoindole-1,3(2H)-dione

2-(Chloromethyl)-1H-isoindole-1,3(2H)-dione structure

2-(Chloromethyl)-1H-isoindole-1,3(2H)-dione 

structure
  • CAS No:

    17564-64-6

  • Formula:

    C9H6ClNO2

  • Chemical Name:

    2-(Chloromethyl)-1H-isoindole-1,3(2H)-dione

  • Synonyms:

    1H-Isoindole-1,3(2H)-dione,2-(chloromethyl)-;Phthalimide,N-(chloromethyl)-;2-(Chloromethyl)-1H-isoindole-1,3(2H)-dione;N-(Chloromethyl)phthalimide;Chloromethylphthalimide;NSC 29558;Phthalimidomethyl chloride;2-(Chloromethyl)isoindoline-1,3-dione;2-(Chloromethyl)isoindole-1,3-dione;2-(Chloromethyl)-2,3-dihydro-1H-isoindole-1,3-dione

  • Categories:

    Chemical Reagents  >  Organic Reagents

Description

white crystalline powder

2-(Chloromethyl)-1H-isoindole-1,3(2H)-dione Basic Attributes

195.6

195.60

140942

241-541-4

N45CYY145E

29558

DTXSID3027790

29251995

Characteristics

37.4

2.2

White powder.

1.3228 (rough estimate)

153 °C

305.2±25.0 °C(Predicted)

138.4±23.2 °C

1.5790 (estimate)

H2O: slightly soluble ;chloroform: soluble 50mg/mL

Store in a tightly closed container. Store in a cool, dry, well-ventilated area away from incompatible substances.

Safety Information

UN 2811 6.1 / PGIII

3

36/37/38-52/53-43-22

26-36-37/39-61-45

Xi,Xn

Stable at room temperature in closed containers under normal storage and handling conditions.

P261-P280-P301 + P310-P305 + P351 + P338

H301-H315-H317-H319-H335

|Danger|H301 (49.37%): Toxic if swallowed [Danger Acute toxicity, oral]|P261, P264, P270, P271, P272, P280, P301+P310, P302+P352, P304+P340, P305+P351+P338, P312, P321, P330, P332+P313, P333+P313, P337+P313, P362, P363, P403+P233, P405, and P501|Aggregated GHS information provided by 79 companies from 4 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.

2-(Chloromethyl)-1H-isoindole-1,3(2H)-dione Use and Manufacturing

Methods of Manufacturing

After phthalimide is obtained by the reaction of phthalic anhydride and ammonium bicarbonate, it is obtained by hydroxylation and chlorination. 1. Preparation of phthalimide: Phthalic anhydride and ammonium bicarbonate are reacted to obtain phthalimide. 2. Preparation of N-hydroxymethyl phthalimide N-hydroxymethyl phthalimide is obtained by reacting formaldehyde with phthalimide. 3. Preparation of chloromethylbenzimide N-chloromethylbenzimide is prepared from N-hydroxymethylphthalimide.

Uses

Pesticide intermediates.

1H-Isoindole-1,3(2H)-dione, 2-(chloromethyl)-: ACTIVE

Computed Properties

Molecular Weight:195.60
XLogP3:2.2
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:1
Exact Mass:195.0087061
Monoisotopic Mass:195.0087061
Topological Polar Surface Area:37.4
Heavy Atom Count:13
Complexity:230
Covalently-Bonded Unit Count:1
Compound Is Canonicalized:Yes

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