p-Toluenesulfonyl hydrazide - CAS 1576-35-8

Name: p-Toluenesulfonyl hydrazide
Brand: BOC Sciences
Rating: 5 (1 reviews)

Catalog:	BB011335
Product Name:	p-Toluenesulfonyl hydrazide
CAS:	1576-35-8
Synonyms:	4-methylbenzenesulfonohydrazide

Technical Data

IUPAC Name:	4-methylbenzenesulfonohydrazide
Description:	p-Toluenesulfonyl hydrazide (CAS# 1576-35-8) is a reactant that has been used in the synthesis of paspaline.
Molecular Weight:	186.23
Molecular Formula:	C7H10N2O2S
Canonical SMILES:	CC1=CC=C(C=C1)S(=O)(=O)NN
InChI:	InChI=1S/C7H10N2O2S/c1-6-2-4-7(5-3-6)12(10,11)9-8/h2-5,9H,8H2,1H3
InChI Key:	ICGLPKIVTVWCFT-UHFFFAOYSA-N
Melting Point:	109-113°C
Purity:	98 %
Density:	1.42 g/cm³
Appearance:	White to off-white powder
Storage:	Flammables area
MDL:	MFCD00007588
LogP:	2.31900
Refractive Index:	1.576
Stability:	Stable under normal temperatures and pressures.

GHS Hazard Statement:	H242 (38.95%): Heating may cause a fire [Danger Self-reactive substances and mixtures; Organic peroxides]
Precautionary Statement:	P201, P202, P210, P220, P234, P260, P261, P264, P270, P272, P273, P280, P281, P301+P310, P301+P312, P302+P352, P305+P351+P338, P308+P313, P314, P321, P330, P332+P313, P333+P313, P337+P313, P362, P363, P370+P378, P391, P403+P235, P405, P411, P420, and P501
Signal Word:	Danger

Publication Number	Title	Priority Date
US-11040939-B1	N-transfer reagent and method for preparing the same and its application	20200623
WO-2021125229-A1	Indazole compound or salt thereof, and pharmaceutical composition	20191217
WO-2021127166-A1	Inhibitors of enl/af9 yeats	20191217
WO-2021121294-A1	Triazolopyridazine derivative, preparation method therefor, pharmaceutical composition thereof, and use thereof	20191216
WO-2021112496-A1	Heterocyclic compound and organic light-emitting device comprising same	20191202

PMID	Publication Date	Title	Journal
22846058	20120817	Protecting-group-free synthesis of glycosyl 1-phosphates	Organic letters
22785266	20120711	Synthesis of new 1,3,4-thiadiazole and 1,2,3,4-oxathiadiazole derivatives from carbohydrate precursors and study of their effect on tyrosinase enzyme	Molecules (Basel, Switzerland)
22475034	20120420	Conformations and reactions of bicyclo[3.2.1]oct-6-en-8-ylidene	The Journal of organic chemistry
21831320	20110811	Catabolic regulation analysis of Escherichia coli and its crp, mlc, mgsA, pgi and ptsG mutants	Microbial cell factories
21906371	20110713	Implications of various phosphoenolpyruvate-carbohydrate phosphotransferase system mutations on glycerol utilization and poly(3-hydroxybutyrate) accumulation in Ralstonia eutropha H16	AMB Express

Complexity:	224
Compound Is Canonicalized:	Yes
Covalently-Bonded Unit Count:	1
Defined Atom Stereocenter Count:	0
Defined Bond Stereocenter Count:	0
Exact Mass:	186.04629874
Formal Charge:	0
Heavy Atom Count:	12
Hydrogen Bond Acceptor Count:	4
Hydrogen Bond Donor Count:	2
Isotope Atom Count:	0
Monoisotopic Mass:	186.04629874
Rotatable Bond Count:	2
Topological Polar Surface Area:	80.6 Å²
Undefined Atom Stereocenter Count:	0
Undefined Bond Stereocenter Count:	0
XLogP3:	0.2