ABCN: Difference between revisions

Browse history interactively ← Previous edit Next edit →Content deleted Content addedVisual WikitextInline

Revision as of 09:05, 30 December 2021 editVedicoy (talk \| contribs)59 editsmNo edit summary← Previous edit		Revision as of 17:25, 17 February 2022 edit undoM97uzivatel (talk \| contribs)Extended confirmed users6,582 editsNo edit summaryNext edit →
Line 2:		Line 2:
	{{For\|the Australian TV station\|ABN (TV station)}}		{{For\|the Australian TV station\|ABN (TV station)}}
	{{Chembox		{{Chembox
	\| Verifiedfields = changed		\|Verifiedfields = changed
	\| Watchedfields = changed		\|Watchedfields = changed
	\| verifiedrevid = 477235009		\|verifiedrevid = 477235009
	\| ImageFile1 = ABCN-2D-skeletal.png		\|ImageFile1 = ABCN-2D-skeletal.png
	\| ImageFile1_Ref = {{chemboximage\|correct\|??}}		\|ImageFile1_Ref = {{chemboximage\|correct\|??}}
		⚫	\|ImageName1 = Stereo, skeletal formula of (''Z'')-ABCN
	\| ImageSize1 =
		⚫	\|ImageFile2 = ABCN-3D-sticks.png
⚫	\| ImageName1 = Stereo, skeletal formula of (''Z'')-ABCN
		⚫	\|ImageFile2_Ref = {{chemboximage\|correct\|??}}
⚫	\| ImageFile2 = ABCN-3D-sticks.png
		⚫	\|ImageName2 = Stick model of (''Z'')-ABCN
⚫	\| ImageFile2_Ref = {{chemboximage\|correct\|??}}
		⚫	\|ImageFile3 = ABCN-3D-vdW.png
	\| ImageSize2 =
		⚫	\|ImageFile3_Ref = {{chemboximage\|correct\|??}}
⚫	\| ImageName2 = Stick model of (''Z'')-ABCN
		⚫	\|ImageName3 = Spacefill model of (''Z'')-ABCN
⚫	\| ImageFile3 = ABCN-3D-vdW.png
		⚫	\|SystematicName = 1,1′-Diazene-1,2-diyldicyclohexanecarbonitrile
⚫	\| ImageFile3_Ref = {{chemboximage\|correct\|??}}
	\| ImageSize3 =
⚫	\| ImageName3 = Spacefill model of (''Z'')-ABCN
⚫	\| SystematicName = 1,1′-Diazene-1,2-diyldicyclohexanecarbonitrile
	\|Section1={{Chembox Identifiers		\|Section1={{Chembox Identifiers
	\| Abbreviations = ACHN		\|Abbreviations = ACHN
	\| CASNo_Ref = {{cascite\|correct\|CAS}}		\|CASNo_Ref = {{cascite\|correct\|CAS}}
	\| CASNo = 2094-98-6		\|CASNo = 2094-98-6
	\| UNII_Ref = {{fdacite\|correct\|FDA}}		\|UNII_Ref = {{fdacite\|correct\|FDA}}
	\| UNII = 9Y0B93KKUS		\|UNII = 9Y0B93KKUS
	\| PubChem = 74978		\|PubChem = 74978
	\| ChemSpiderID = 21159585		\|ChemSpiderID = 21159585
	\| ChemSpiderID_Ref = {{chemspidercite\|correct\|chemspider}}		\|ChemSpiderID_Ref = {{chemspidercite\|correct\|chemspider}}
	\| ChemSpiderID2 = 21427655		\|ChemSpiderID2 = 21427655
	\| ChemSpiderID2_Ref = {{chemspidercite\|correct\|chemspider}}		\|ChemSpiderID2_Ref = {{chemspidercite\|correct\|chemspider}}
	\| ChemSpiderID2_Comment = <small>(''Z'')</small>		\|ChemSpiderID2_Comment = <small>(''Z'')</small>
	\| ChemSpiderID1 = 67533		\|ChemSpiderID1 = 67533
	\| ChemSpiderID1_Ref = {{chemspidercite\|correct\|chemspider}}		\|ChemSpiderID1_Ref = {{chemspidercite\|correct\|chemspider}}
	\| ChemSpiderID1_Comment = <small>(''E'')</small>		\|ChemSpiderID1_Comment = <small>(''E'')</small>
	\| EINECS = 218-254-8		\|EINECS = 218-254-8
	\| UNNumber = 3226		\|UNNumber = 3226
	\| Beilstein = 960744		\|Beilstein = 960744
	\| SMILES = N#CC1(CCCCC1)N=NC1(CCCCC1)C#N		\|SMILES = N#CC1(CCCCC1)N=NC1(CCCCC1)C#N
	\| StdInChI = 1S/C14H20N4/c15-11-13(7-3-1-4-8-13)17-18-14(12-16)9-5-2-6-10-14/h1-10H2		\|StdInChI = 1S/C14H20N4/c15-11-13(7-3-1-4-8-13)17-18-14(12-16)9-5-2-6-10-14/h1-10H2
	\| StdInChI_Ref = {{stdinchicite\|correct\|chemspider}}		\|StdInChI_Ref = {{stdinchicite\|correct\|chemspider}}
	\| InChI = 1/C14H20N4/c15-11-13(7-3-1-4-8-13)17-18-14(12-16)9-5-2-6-10-14/h1-10H2		\|InChI = 1/C14H20N4/c15-11-13(7-3-1-4-8-13)17-18-14(12-16)9-5-2-6-10-14/h1-10H2
	\| StdInChIKey = KYIKRXIYLAGAKQ-UHFFFAOYSA-N		\|StdInChIKey = KYIKRXIYLAGAKQ-UHFFFAOYSA-N
	\| StdInChIKey_Ref = {{stdinchicite\|correct\|chemspider}}		\|StdInChIKey_Ref = {{stdinchicite\|correct\|chemspider}}
	\| InChIKey = KYIKRXIYLAGAKQ-UHFFFAOYAM		\|InChIKey = KYIKRXIYLAGAKQ-UHFFFAOYAM
	}}		}}
	\|Section2={{Chembox Properties		\|Section2={{Chembox Properties
	\| C=14 \| H=20 \| N=4		\|C=14 \| H=20 \| N=4
	\| MeltingPtC = 114 to 118<ref name=SA> at ]</ref>		\|MeltingPtC = 114 to 118<ref name=SA> at ]</ref>
	\| MeltingPt_notes = decomposes near 80 °C		\|MeltingPt_notes = decomposes near 80 °C
	}}		}}
	\|Section3={{Chembox Hazards		\|Section3={{Chembox Hazards
	\| GHSPictograms = {{GHS flame}} {{GHS exclamation mark}}		\|GHSPictograms = {{GHS flame}} {{GHS exclamation mark}}
	\| GHSSignalWord = Danger		\|GHSSignalWord = Danger
	\| HPhrases = {{H-phrases\|242\|315\|319\|335}}		\|HPhrases = {{H-phrases\|242\|315\|319\|335}}
	\| PPhrases = {{P-phrases\|261\|305+351+338}}		\|PPhrases = {{P-phrases\|261\|305+351+338}}
	}}		}}
	}}		}}

Revision as of 17:25, 17 February 2022

For Indian IT Company Abcence, see Abcence. For the Australian TV station, see ABN (TV station).

ABCN
Names



Systematic IUPAC name 1,1′-Diazene-1,2-diyldicyclohexanecarbonitrile
Identifiers
CAS Number	2094-98-6
3D model (JSmol)	Interactive image
Abbreviations	ACHN
Beilstein Reference	960744
ChemSpider	21159585 67533 (E) 21427655 (Z)
ECHA InfoCard	100.016.595
EC Number	218-254-8
PubChem CID	74978
UNII	9Y0B93KKUS
UN number	3226
CompTox Dashboard (EPA)	DTXSID9044613
InChI InChI=1S/C14H20N4/c15-11-13(7-3-1-4-8-13)17-18-14(12-16)9-5-2-6-10-14/h1-10H2Key: KYIKRXIYLAGAKQ-UHFFFAOYSA-N InChI=1/C14H20N4/c15-11-13(7-3-1-4-8-13)17-18-14(12-16)9-5-2-6-10-14/h1-10H2Key: KYIKRXIYLAGAKQ-UHFFFAOYAM
SMILES N#CC1(CCCCC1)N=NC1(CCCCC1)C#N
Properties
Chemical formula	C₁₄H₂₀N₄
Molar mass	244.342 g·mol
Melting point	114 to 118 °C (237 to 244 °F; 387 to 391 K) decomposes near 80 °C
Hazards
GHS labelling:
Pictograms
Signal word	Danger
Hazard statements	H242, H315, H319, H335
Precautionary statements	P261, P305+P351+P338
Except where otherwise noted, data are given for materials in their standard state (at 25 °C , 100 kPa). N verify (what is ?) Infobox references

Chemical compound

1,1′-Azobis(cyclohexanecarbonitrile) or ACHN is a radical initiator. The molecular formula is NCC₆H₁₀N=NC₆H₁₀CN. It is a white solid that is soluble in aromatic solvents.

ACHN has a 10-hour half-life in toluene at 88 °C.

References

^ 1,1′-Azobis(cyclohexanecarbonitrile) at Sigma-Aldrich
Steven A. Kates, Fernando Albericio (2001). "1,1'-Azobis-1-cyclohexanenitrile". E-EROS Encyclopedia of Reagents for Organic Synthesis. doi:10.1002/047084289X.ra120.

This article about an organic compound is a stub. You can help Misplaced Pages by expanding it.

Categories:

Revision as of 17:25, 17 February 2022

See also

References