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线性分子式:
(CH3)2NC6H4CN
化学文摘社编号:
分子量:
146.19
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
214-819-8
Beilstein/REAXYS Number:
971606
MDL number:
产品名称
4-(二甲氨基)苯甲腈, 98%
InChI key
JYMNQRQQBJIMCV-UHFFFAOYSA-N
InChI
1S/C9H10N2/c1-11(2)9-5-3-8(7-10)4-6-9/h3-6H,1-2H3
SMILES string
CN(C)c1ccc(cc1)C#N
assay
98%
form
crystals
bp
318 °C (lit.)
mp
72-75 °C (lit.)
Quality Level
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Application
4-(二甲胺基)苄腈可用于合成3,6-二苯基-2,5-二氢-吡咯并[3,4-c]吡咯-1,4-二酮衍生物。
General description
4-(二甲胺基)苄腈在光激发下可以发生从二甲基氨基部分到氰基苯基部分的分子内电荷转移(ICT),导致出现双重荧光,因此,它被广泛用于光物理研究。
signalword
Warning
hcodes
Hazard Classifications
Acute Tox. 4 Oral - Eye Irrit. 2 - Skin Irrit. 2 - Skin Sens. 1 - STOT SE 3
target_organs
Respiratory system
存储类别
11 - Combustible Solids
wgk
WGK 2
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Faceshields, Gloves
Do fluorescence and transient absorption probe the same intramolecular charge transfer state of 4-(dimethylamino) benzonitrile?
Gustavsson T, et al.
J. Chem. Phys. , 131, 031101-031101 (2009)
D H Hutson et al.
Xenobiotica; the fate of foreign compounds in biological systems, 14(12), 925-934 (1984-12-01)
4-Cyano-N,N-dimethylaniline (CDA), when administered to rats as a single oral dose (18.5 mg/kg), was rapidly absorbed and eliminated as a mixture of metabolites in the urine (86% dose after 24 h). Residues in tissues after 48 h, expressed as microgram
Novel, soluble diphenyl-diketo-pyrrolopyrroles: Experimental and theoretical study.
Vala M, et al.
Dyes and Pigments, 84(2), 176-182 (2010)
D Hesk et al.
Xenobiotica; the fate of foreign compounds in biological systems, 18(8), 955-966 (1988-08-01)
1. The metabolic fate of 4-cyanoacetanilide (CAA), labelled with 14C and 13C in the N-acetyl group, was studied in rats (oral dose, 22.5 mg/kg) and mice (oral dose 21.7 mg/kg). 2. The metabolic profile in the urine of rats was
C J Logan et al.
Xenobiotica; the fate of foreign compounds in biological systems, 15(5), 391-397 (1985-05-01)
4-Cyano-N,N-dimethylaniline (CDA), when administered as a single oral dose to mice (18.5 mg/kg), was rapidly absorbed and eliminated. The major route of elimination was the urine (78% dose in 24h). The residues in the tissues 48 h after dosing, as
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