Detail of "10272-07-8"

CAS Number:
10272-07-8
Name:
3,5-Dimethoxyaniline
Molecular Structure:
Formula:
C₈H₁₁NO₂
Molecular Weight:
153.18
Synonyms:
3,5-Dimethoxy-phenylamine;3,5-Dimethoxybenzeneamine;Benzenamine, 3,5-dimethoxy-;3，5-dimethoxy aniline;5-Aminoresorcinol dimethylether;
EINECS:
233-616-5
Density:
1.096 g/cm³
Melting Point:
54-57 ºC
Boiling Point:
178 ºC (20 mmHg)
Flash Point:
135 ºC
Solubility:
insoluble in water
Appearance:
White crystal or Colorless liquid
Hazard Symbols:
Xn,Xi
Risk Codes:
22-36/37/38-20/21/22
Safety:
26-36-36/37/39-22 Details
Transport Information:
UN 2811

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Substituted pyrazinecarboxamides: synthesis and biological evaluation: All Rights Reserved.Some chemicals with cas registry numbers like 1603-91-4 and 10272-07-8 are also used. Substituted pyrazinecarboxamides: synthesis and biological evaluation. Dolezal, Martin; Palek, Lukas; Vinsova, Jarmila; Buchta, Vladimir; Jampilek, Josef; Kralova, Katarina (Faculty of Pharmacy in Hradec Kralove, Charles University in Prague, Hradec Kralove 500 05, Czech Rep.). Molecules, 11(4), 242-256 (English) 2006 Molecular Diversity Preservation International. URL: http://www.mdpi.org/molecules/papers/11040242.pdf. CODEN: MOLEFW. ISSN: 1420-3049. DOCUMENT TYPE: Journal; (online computer file) CA Section: 28 (Heterocyclic Compounds (More Than One Hetero Atom)) Section cross-reference(s): 1, 11 Condensation of the acid chlorides of some substituted pyrazine-2-carboxylic acids (pyrazine-2-carboxylic acid, 6-chloropyrazine-2-carboxylic acid, 5-tert-butylpyrazine-2-carboxylic acid or 5-tert-butyl-6-chloropyrazine-2-carboxylic acid) with various ring-substituted aminothiazoles or anilines yielded a series of amides. The syntheses, anal. and spectroscopic data of thirty newly prepd. compds. are presented. Structure-activity relationships between the chem. structures and the antimycobacterial, antifungal and photosynthesis-inhibiting activity of the evaluated compds. are discussed. 3,5-Bromo-4-hydroxyphenyl derivs. of substituted pyrazinecarboxylic acid have shown the highest activity against Mycobacterium tuberculosis H37Rv (54-72% inhibition). The highest antifungal effect against Trichophyton mentagrophytes, the most susceptible fungal strain tested, was found for 5-tert-butyl-6-chloro-N-(4-methyl-1,3-thiazol-2-yl)pyrazine-2-carboxamid e (I, MIC = 31.25 mmol×mL-1). The most active inhibitors of oxygen evolution rate in spinach chloroplasts were 5-tert-butyl-6-chloro-N-(5-bromo-2-hydroxyphenyl)pyrazine-2-carboxami de (II, IC50 = 41.9 mmol×L-1) and 5-tert-butyl-6-chloro-N-(1,3-thiazol-2-yl)pyrazine-2-carboxamide (IC50 = 49.5 mmol×L-1). .

Synthesis of analogs of glycozolidine: Synthesis of analogs of glycozolidine. Bhattacharyya, P.; Basak, S. P.; Islam, A.; Chakraborty, D. P.There are some reagents with their cas registry numbers 10272-07-8 and 62069-65-2 are used in this study. (Bose Inst., Calcutta, India). J. Indian Chem. Soc., 53(8), 861-3 (English) 1976. CODEN: JICSAH. DOCUMENT TYPE: Journal CA Section: 31 (Alkaloids) Section cross-reference(s): 27 The glycozolidine analogs I (R = R2 = MeO, R1 = H; R = H, R1 = R2 = MeO) were prepd. by condensation of 2-(hydroxymethylene)-5-methylcyclohexanone with 3,4,5-RR1R2C6H2NH2.HCl followed by cyclization of the hydrazones to give the carbazoles II, which were reduced and dehydrogenated. .

Detail of "10272-07-8"

3,5-Dimethoxyaniline

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CAS No.10272-07-8 3,5-Dimethoxyaniline

CAS No.10272-07-8 3,5-Dimethoxyaniline

CAS No.10272-07-8 3,5-Dimethoxyaniline

CAS No.10272-07-8 3,5-Dimethoxyaniline

CAS No.10272-07-8 3,5-Dimethoxyaniline

CAS No.10272-07-8 3,5-Dimethoxyaniline

CAS No.10272-07-8 3,5-Dimethoxyaniline

Reference