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Merck
CN

232424

N-(Chloromethyl)phthalimide

97%

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About This Item

Empirical Formula (Hill Notation):
C9H6ClNO2
CAS Number:
17564-64-6
Molecular Weight:
195.60
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
24853898
EC Number:
241-541-4
Beilstein/REAXYS Number:
140942
MDL number:
MFCD00005898
Assay:
97%
Form:
powder

Key Documents

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InChI key

JKGLRGGCGUQNEX-UHFFFAOYSA-N

InChI

1S/C9H6ClNO2/c10-5-11-8(12)6-3-1-2-4-7(6)9(11)13/h1-4H,5H2

SMILES string

ClCN1C(=O)c2ccccc2C1=O

assay

97%

form

powder

Quality Level

200

solubility

chloroform: soluble 50 mg/mL

functional group

chloro, imide

Related Categories

Application

N-(Chloromethyl)phthalimide 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),11,14-trien-19-oicacid, new labdane-type diterpenoid

pictograms

Skull and crossbones
GHS06

signalword

Danger

Hazard Classifications

Acute Tox. 3 Oral - Eye Irrit. 2 - Skin Irrit. 2 - Skin Sens. 1 - STOT SE 3

target_organs

Respiratory system

Storage Class

6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Faceshields, Gloves

Regulatory Information

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Certificates of Analysis (COA)

Lot/Batch Number
BCBZ3613
BCBS1376V
BCBB1162V
BCBB1162
02730JJ

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Preparation of high capacity aminomethyl-polystyrene resin.
Zikos CC and Ferderigos NG.
Tetrahedron Letters, 36(21), 3741-3744 (1995)
M Iwamoto et al.
Bioorganic & medicinal chemistry, 9(7), 1911-1921 (2001-06-27)
Three new labdane-type diterpenoids, labda-8(17),13-dien-15,12R-olid-19-oic acid (1), 12S-hydroxylabda-8(17),13(16),14-trien-19-oic acid (2) and 13-ethoxylabda-8(17),11,14-trien-19-oic acid (3), along with known diterpenoids, trans-communic acid (4), totarol (5), 12-methoxyabieta-8,11,13-trien-11-ol (6), and 7 alpha,8 alpha-epoxy-6 alpha-hydroxyabieta-9(11),13-dien-12-one (7) were isolated from the stem bark of Thuja standishii.

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