283541
4-硝基苯基异硫氰酸酯
98%
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关于此项目
线性分子式:
O2NC6H4NCS
化学文摘社编号:
分子量:
180.18
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
218-359-9
Beilstein/REAXYS Number:
640027
MDL number:
产品名称
4-硝基苯基异硫氰酸酯, 98%
InChI key
NXHSSIGRWJENBH-UHFFFAOYSA-N
InChI
1S/C7H4N2O2S/c10-9(11)7-3-1-6(2-4-7)8-5-12/h1-4H
SMILES string
[O-][N+](=O)c1ccc(cc1)N=C=S
assay
98%
form
powder
bp
137-138 °C/11 mmHg (lit.)
mp
110-112 °C (lit.)
functional group
isothiocyanate
nitro
Quality Level
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Application
4-Nitrophenyl isothiocyanate has been used in the synthesis of:
- 5,6-dimethyl-2-[(4-nitrophenyl)amino]thieno[2,3-d]pyrimidin-4(3H)-one
- 4,5-dimethyl-2-substituted carbamothioylaminothiophene-3-carboxamides
- acyclic triazene or zwitterionic dihydropyrimidinium imidothiolate derivatives
General description
The solid-state reactivity of hydrazine hydrochloride with 4-nitrophenyl isothiocyanate was studied.
signalword
Danger
hcodes
Hazard Classifications
Eye Irrit. 2 - Resp. Sens. 1 - Skin Irrit. 2 - Skin Sens. 1 - STOT SE 3
target_organs
Respiratory system
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Faceshields, Gloves
Investigation into the reaction of 2-amino-4, 5-dimethylthiophene-3-carboxamide with iso (and isothio) cyanates under microwave irradiation.
Davoodnia A, et al.
Heteroatom Chem., 20(6), 346-349 (2009)
Solid?state reactivity of the hydrazine?hydroquinone complex.
Kaupp G and Schmeyers J.
Journal of Physical Organic Chemistry, 13(7), 388-394 (2000)
Exploring the nucleophilicity of N, N'-diamidocarbenes: Heteroallenes and related compounds as coupling reagents.
Lee YG, et al.
Journal of Physical Organic Chemistry, 25(11), 1027-1027 (2012)
Nargess Yousefi Limaee et al.
Journal of fluorescence, 30(2), 375-387 (2020-02-23)
Fluorescent molecularly imprinted polymer (FMIP) optosensor was utilized for the selective identification of 2,4-dichlorophenoxacetic acid (2,4-D) due to worldwide pollution caused by using herbicides in agricultural industry. In this regards, two derivatives of polymerizable 1,8-naphthalimide namely, 1,8-naphthalimide containing thiourea (NI)
Junta Sano et al.
Polymers, 12(5) (2020-05-24)
Novel interpenetrating polymer networks (IPNs) were synthesized from N-isopropylacrylamide (NIPAM) and polysiloxanes containing a urea or thiourea side group, in addition to the silanol residue, through two reactions, such as the radical gelation of NIPAM and the condensation of silanols
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