31:
381:
465:
Schwarzenbach, Gerold; Bürgi, Hans-Beat; Jensen, William P.; Lawrance, Geoffrey A.; Mønsted, Lene; Sargeson, Alan M. (1983). "Acid cleavage of nickel(II) complexes containing
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438:-1,3,5-triaminocyclohexane. Synthesis of novel hexadentate ligand derivatives for the preparation of gallium radiopharmaceuticals".
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43:
8:
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481:, and a correlation between the structure and reactivity of nickel–polyamine complexes".
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Bowen, Tom; Planalp, Roy P.; Brechbiel, Martin W. (1996). "An improved synthesis of
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Structure of (color code: blue = nitrogen, red = oxygen; dark blue = nickel).
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Except where otherwise noted, data are given for materials in their
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343:
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354:-1,3,5-derivative has attracted attention because it is a common
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362:. It is a colorless oil. It is a popular tridentate ligand in
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InChI=1S/C6H15N3/c7-4-1-5(8)3-6(9)2-4/h4-6H,1-3,7-9H2/t4-,5+,6-
112:
346:. Of the many isomers possible for triaminocyclohexane, the
473:-1,3,5-cyclohexanetriamine (TACH), crystal structure of (NO
380:
429:
505:
373:of cyclohexane. The latter is generated via the
167:
377:starting from cyclohexanetricarboxylic acid.
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440:Bioorganic & Medicinal Chemistry Letters
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379:
506:
284:285 °C (545 °F; 558 K)
194:Key: UYAUGHKQCCCFDK-FPFOFBBKSA-N
158:
13:
388:
14:
530:
248:
242:
29:
397:, another tripodal triamine (CH
294:(at 25 °C , 100 kPa).
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423:
236:
1:
417:
452:10.1016/0960-894X(96)00110-2
369:It is prepared from the tris
60:)-Cyclohexane-1,3,5-triamine
7:
77:-Cyclohexane-1,3,5-triamine
24:-1,3,5-Triaminocyclohexane
10:
535:
324:-1,3,5-Triaminocyclohexane
308:
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82:
66:
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28:
309:Not to be confused with
395:Tris(aminomethyl)ethane
385:
364:coordination chemistry
383:
375:Curtius rearrangement
330:with the formula (CH
44:Preferred IUPAC name
495:10.1021/ic00168a042
483:Inorganic Chemistry
266: g·mol
25:
386:
298:Infobox references
16:
489:(26): 4029–4038.
358:, abbreviated as
311:triazacyclohexane
306:Chemical compound
304:
303:
274:Colorless liquid
124:Interactive image
526:
514:Tripodal ligands
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328:organic compound
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231:Chemical formula
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389:Related ligands
356:tripodal ligand
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446:(7): 807–810.
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292:standard state
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280:Boiling point
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215:C1(C(C1N)N)N
83:Identifiers
74:
70:
67:Other names
57:
53:
49:
21:
17:
342:. It is a
271:Appearance
224:Properties
519:Polyamines
508:Categories
418:References
259:Molar mass
135:ChemSpider
111:3D model (
100:26150-46-9
90:CAS Number
371:carbamate
344:triamine
144:19549297
264:129.207
156:PubChem
326:is an
208:SMILES
169:427712
69:TACH;
38:Names
183:InChI
113:JSmol
401:C(CH
360:tach
334:CHNH
491:doi
471:cis
467:cis
448:doi
436:cis
432:cis
352:cis
348:cis
322:cis
318:cis
159:CID
75:cis
71:cis
22:cis
18:cis
510::
487:22
485:.
442:.
405:NH
366:.
246:15
56:,5
52:,3
48:(1
497:.
493::
479:2
477:)
475:3
469:,
454:.
450::
444:6
434:,
413:)
411:3
409:]
407:2
403:2
399:3
350:,
340:3
338:)
336:2
332:2
320:,
313:.
252:3
249:N
243:H
240:6
237:C
115:)
73:,
58:s
54:s
50:s
20:,
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