1-Nitro-2-tosylbenzene - CAS 1220-92-4

Catalog:	BB005335
Product Name:	1-Nitro-2-tosylbenzene
CAS:	1220-92-4
Synonyms:	1-(4-methylphenyl)sulfonyl-2-nitrobenzene; 1-(4-methylphenyl)sulfonyl-2-nitrobenzene

Technical Data

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Computed Properties

IUPAC Name:	1-(4-methylphenyl)sulfonyl-2-nitrobenzene
Description:	1-Nitro-2-tosylbenzene (CAS# 1220-92-4 ) is a useful research chemical.
Molecular Weight:	277.30
Molecular Formula:	C13H11NO4S
Canonical SMILES:	CC1=CC=C(C=C1)S(=O)(=O)C2=CC=CC=C2[N+](=O)[O-]
InChI:	InChI=1S/C13H11NO4S/c1-10-6-8-11(9-7-10)19(17,18)13-5-3-2-4-12(13)14(15)16/h2-9H,1H3
InChI Key:	JPGVTAXHQBLUJH-UHFFFAOYSA-N
LogP:	4.34000

Publication Number	Title	Priority Date
CN-112574077-A	Method for synthesizing sulfone compound under photocatalysis condition	20201212
US-2009092931-A1	Methods of forming a blocking pattern using a photosensitive composition and methods of manufacturing a semiconductor device	20070814
US-2003148212-A1	Process for forming an ultra fine pattern using a bottom anti-reflective coating film containing an acid generator	20011218
US-2006183050-A1	Process for forming an ultra fine pattern using a bottom anti-reflective coating film containing an acid generator	20011218
US-7138218-B2	Process for forming an ultra fine pattern using a bottom anti-reflective coating film containing an acid generator	20011218

PMID	Publication Date	Title	Journal
7684215	19930401	Diarylsulfones, a new chemical class of nonnucleoside antiviral inhibitors of human immunodeficiency virus type 1 reverse transcriptase	Antimicrobial agents and chemotherapy

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Complexity:	415
Compound Is Canonicalized:	Yes
Covalently-Bonded Unit Count:	1
Defined Atom Stereocenter Count:	0
Defined Bond Stereocenter Count:	0
Exact Mass:	277.04087901
Formal Charge:	0
Heavy Atom Count:	19
Hydrogen Bond Acceptor Count:	4
Hydrogen Bond Donor Count:	0
Isotope Atom Count:	0
Monoisotopic Mass:	277.04087901
Rotatable Bond Count:	2
Topological Polar Surface Area:	88.3
Undefined Atom Stereocenter Count:	0
Undefined Bond Stereocenter Count:	0
XLogP3:	2.9