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238627

Sigma-Aldrich

Ethyl isocyanatoacetate

95%

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About This Item

Linear Formula:
OCNCH2COOCH2CH3
CAS Number:
Molecular Weight:
129.11
Beilstein:
970503
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

Assay

95%

form

liquid

impurities

<5% N-(chloroformyl)glycine ethyl ester

refractive index

n20/D 1.422 (lit.)

bp

67-68 °C/11 mmHg (lit.)

density

1.151 g/mL at 25 °C (lit.)

SMILES string

CCOC(=O)CN=C=O

InChI

1S/C5H7NO3/c1-2-9-5(8)3-6-4-7/h2-3H2,1H3

InChI key

DUVOZUPPHBRJJO-UHFFFAOYSA-N

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Application

Ethyl isocyanatoacetate has been used in the preparation of:
  • 6-(carboxymethylureido)-(±)-nicotine (CMUNic), nicotine immunogen
  • ethyl 8-carbamoyl-4-oxo-3,4-dihydroimidazo[5,1-d]-1,2,3,5-tetrazin-3-ylacetate
  • imidazo[1,2-c]-quinazoline-2,5-(3H,6H)dione

Pictograms

Health hazardExclamation mark

Signal Word

Danger

Hazard Classifications

Acute Tox. 4 Oral - Eye Irrit. 2 - Resp. Sens. 1 - Skin Irrit. 2 - Skin Sens. 1 - STOT SE 3

Target Organs

Respiratory system

Storage Class Code

10 - Combustible liquids

WGK

WGK 3

Flash Point(F)

161.6 °F - closed cup

Flash Point(C)

72 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

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Antitumour imidazotetrazines. Part 33. New syntheses of the antitumour drug temozolomide using 'masked'methyl isocyanates.
Malcolm FG.
Journal of the Chemical Society. Perkin Transactions 1, 21, 2783-2787 (1995)
A Facile Synthesis of Imidazo [1, 2-c] quinazoline-2, 5-(3H, 6H) dione.
Papadopoulos EP.
Journal of Heterocyclic Chemistry, 18(3), 515-518 (1981)
Y Hieda et al.
The Journal of pharmacology and experimental therapeutics, 283(3), 1076-1081 (1998-02-12)
The ability of active immunization to alter nicotine distribution was studied in rats. Animals were immunized with 6-(carboxymethylureido)-(+/-)-nicotine (CMUNic) linked to keyhole limpet hemocyanin (KLH). Antibody titers determined by ELISA, using CMUNic coupled to albumin as the coating antigen, were

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