40:
28:
422:'A new reagent for the selective, high-yield N-dealkylation of tertiary amines: improved syntheses of naltrexone and nalbuphine' R. A. Olofson, Jonathan T. Martz, Jean Pierre Senet, Marc Piteau, Thierry Malfroot J. Org. Chem., 1984, 49 (11), pp 2081–2082
261:
403:
399:) are a pair of related chemical compounds. They can be used to form protecting groups and as N-dealkylating agents.
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89:
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Except where otherwise noted, data are given for materials in their
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235:InChI=1S/C3H4Cl2O2/c1-2(4)7-3(5)6/h2H,1H3
211:
245:InChI=1/C3H4Cl2O2/c4-1-2-7-3(5)6/h1-2H2
442:
238:Key: QOPVNWQGBQYBBP-UHFFFAOYSA-N
248:Key: SVDDJQGVOFZBNX-UHFFFAOYAR
195: (2-chloroethyl chloroformate)
187: (1-chloroethyl chloroformate)
173:
161: (2-chloroethyl chloroformate)
153: (1-chloroethyl chloroformate)
101: (2-chloroethyl chloroformate)
93: (1-chloroethyl chloroformate)
13:
38:
26:
14:
461:
307:
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361:(at 25 °C , 100 kPa).
67:2-Chloroethyl carbonochloridate
65:1-Chloroethyl carbonochloridate
425:
416:
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1:
432:Extremely Hazardous Chemicals
409:
7:
46:2-Chloroethyl chloroformate
34:1-Chloroethyl chloroformate
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10:
466:
377:Chloroethyl chloroformates
350:Chloromethyl chloroformate
17:Chloroethyl chloroformate
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404:extremely hazardous
402:They are listed as
331: g·mol
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365:Infobox references
336:Related compounds
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373:Chemical compound
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130:Interactive image
123:Interactive image
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381:chemical formula
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290:Chemical formula
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11:
5:
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450:Chloroformates
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359:standard state
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344:chloroformates
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271:
269:ClC(OC(Cl)C)=O
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406:substances.
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274:ClC(=O)OCCCl
73:Identifiers
283:Properties
62:IUPAC names
410:References
324:Molar mass
213:4D32H07Z9I
141:ChemSpider
110:3D model (
90:50893-53-3
80:CAS Number
444:Category
342:Related
98:627-11-2
171:PubChem
329:142.96
262:SMILES
184:521305
150:454726
56:Names
227:InChI
192:12305
158:11802
112:JSmol
204:UNII
383:: C
174:CID
446::
391:Cl
308:Cl
397:2
395:O
393:2
389:4
387:H
385:3
379:(
317:2
314:O
311:2
305:4
302:H
299:3
296:C
114:)
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