User:RRBinwood/sandbox

*para*-toluenesulfinamide
(R)-p-toluenesulfinamide	(S)-p-toluenesulfinamide
Names
	IUPAC name 4-Methylbenzenesulfinamide
	Other names Davis' sulfinamide; Davis' auxiliary;
Identifiers
CAS Number	247089-85-6 (R)-(-); 188447-91-8 (S)-(+);
3D model (JSmol)	(R/S): Interactive image; (R)-(+): Interactive image; (S)-(-): Interactive image;
PubChem CID	11051888 (R)-(-); 11116285 (S)-(+);
	InChI (R/S): InChI=1S/C7H9NOS/c1-6-2-4-7(5-3-6)10(8)9/h2-5H,8H2,1H3 Key: YNJDSRPIGAUCEE-UHFFFAOYSA-N; (R)-(+): InChI=1S/C7H9NOS/c1-6-2-4-7(5-3-6)10(8)9/h2-5H,8H2,1H3/t10-/m1/s1 Key: YNJDSRPIGAUCEE-SNVBAGLBSA-N; (S)-(-): InChI=1S/C7H9NOS/c1-6-2-4-7(5-3-6)10(8)9/h2-5H,8H2,1H3/t10-/m0/s1 Key: YNJDSRPIGAUCEE-JTQLQIEISA-N;
	SMILES (R/S): CC1=CC=C(S(N)=O)C=C1; (R)-(+): CC1=CC=C([S@](N)=O)C=C1; (S)-(-): CC1=CC=C([S@@](N)=O)C=C1;
Properties
Chemical formula	CH3C6H4S(O)NH2,
Molar mass	155.22 g/mol
Appearance	white to off-white crystalline solid
Melting point	115 to 118 °C (239 to 244 °F; 388 to 391 K)
	Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). verify (what is ?) Infobox references

para-Toluenesulfinamide (also known as p-toluenesulfinamide or Davis' sulfinamide/auxiliary) is an organosulfur compound and a member of the class of sulfinamides. Both enantiomeric forms are commercially available and are used in asymmetric synthesis as chiral auxiliaries.^[1]^[2]^[3] This compound was first introduced in 1997 by Franklin A. Davis et al.^[4]

References[edit]

^ Ellman, J. A. (2003). "Applications of tert-butanesulfinamide in the asymmetric synthesis of amines". Pure and Applied Chemistry. 75: 39–46. doi:10.1351/pac200375010039.
^ Robak, Maryann T.; Herbage, Melissa A.; Ellman, Jonathan A. (2010). "Synthesis and Applications oftert-Butanesulfinamide". Chemical Reviews. 110 (6): 3600–740. doi:10.1021/cr900382t. PMID 20420386.
^ Organic Syntheses, Vol. 82, p.157 (2005). Link
^ Davis, Franklin A.; Reddy, Rajarathnam E.; Szewczyk, Joanna M.; Reddy, G. Venkat; Portonovo, Padma S.; Zhang, Huiming; Fanelli, Dean; Zhou, Ping; Carroll, Patrick J. (1997). "Asymmetric Synthesis and Properties of Sulfinimines (Thiooxime S -Oxides)". The Journal of Organic Chemistry. 62 (8): 2555–2563. doi:10.1021/jo970077e. ISSN 0022-3263.

Category:Sulfinamides Category:Reagents for organic chemistry Category:Tert-butyl compounds

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

[1] Ellman, J. A. (2003). "Applications of tert-butanesulfinamide in the asymmetric synthesis of amines". Pure and Applied Chemistry. 75: 39–46. doi:10.1351/pac200375010039.

[2] Robak, Maryann T.; Herbage, Melissa A.; Ellman, Jonathan A. (2010). "Synthesis and Applications oftert-Butanesulfinamide". Chemical Reviews. 110 (6): 3600–740. doi:10.1021/cr900382t. PMID 20420386.

[3] Organic Syntheses, Vol. 82, p.157 (2005). Link

[4] Davis, Franklin A.; Reddy, Rajarathnam E.; Szewczyk, Joanna M.; Reddy, G. Venkat; Portonovo, Padma S.; Zhang, Huiming; Fanelli, Dean; Zhou, Ping; Carroll, Patrick J. (1997). "Asymmetric Synthesis and Properties of Sulfinimines (Thiooxime S -Oxides)". The Journal of Organic Chemistry. 62 (8): 2555–2563. doi:10.1021/jo970077e. ISSN 0022-3263.

[1]

[2]

[3]

[4]