Detail of "15930-53-7"

MSDS Download
CAS Number:
15930-53-7
Name:
1,3-Benzodioxole-5-carboxaldehyde,6-bromo-
Molecular Structure:
Formula:
C8H5 Br O3
Molecular Weight:
229.03
Synonyms:
Piperonal,6-bromo- (6CI,8CI); 2-Bromo-4,5-(methylenedioxy)benzaldehyde;6-Bromo-1,3-benzodioxole-5-carboxaldehyde; 6-Bromo-3,4-(methylenedioxy)benzaldehyde;6-Bromobenzodioxole-5-carboxaldehyde; 6-Bromopiperonal; NSC 15639
Density:
1.782g/cm³
Melting Point:
128-132 °C(lit.)
Boiling Point:
309.2°Cat760mmHg
Flash Point:
140.8°C
Hazard Symbols:
Risk Codes:
36/37/38
Safety:
Hazard Codes Xi
Risk Statements 36/37/38
Safety Statements 37/39-26
WGK Germany 3

RTECS TO1576250

Hazard Note Irritant
Details

Display：

2-Bromo-4,7-methylenedioxybenzaldehyde

Supplier:Fayeton Inc. [ United States]

590 Integral
590

Tel:858 380 6065

Address:USA

660 Integral
660

Tel:+86-571-82836136-805

Address:room 1502,uint1,bld.2,nan'an bright pearl plaza,xiaoshan economic&technological development zone,hangzhou,311215,china

Please post your buying leads,so that our qualified suppliers will soon contact you!
*Required Fields

Reaction of 3,4-methylenedioxybenzaldehydes with sodium methoxide: Reaction of 3,4-methylenedioxybenzaldehydes with sodium methoxide. Baratov, N. Yu.; Vinogradova, V. I.; Yunusov, M. S. (Inst. Khim. Rastit. Veshchestv, Tashkent, USSR). Zh. Org. Khim., 27(7), 1578-9 (Russian) 1991. CODEN: ZORKAE. ISSN: 0514-7492. DOCUMENT TYPE: Journal CA Section: 28 (Heterocyclic Compounds (More Than One Hetero Atom)) The reaction of benzaldehyde I with NaOMe in DMF in presence of CuCl2 gave methoxybenzaldehydes II (R = MeO, H) in 70% and 62% yield resp. 15930-53-7 and 120-57-0 are just another two chemicals used in this study. The structures of II (R = MeO, H) were confirmed by their synthesis from II (R = Br) and piperonal, resp. .

Dihydrophthalazine antagonists of excitatory amino acid receptors: Dihydrophthalazine antagonists of excitatory amino acid receptors. Pelletier, Jeffrey C. (Symphony Pharmaceuticals, Inc., USA). PCT Int. Appl. WO 9640646 A1 19 Dec 1996, 59 pp. DESIGNATED STATES: W: CA, CN, JP; RW: AT, BE, CH, DE, DK, ES, FI, FR, GB, GR, IE, IT, LU, MC, NL, PT, SE. (English). (World Intellectual Property Organization). CODEN: PIXXD2. CLASS: ICM: C07D237-30. ICS: C07D491-04. APPLICATION: WO 1996-US7598 24 May 1996. PRIORITY: US 1995-476272 7 Jun 1995; US 1996-588145 18 Jan 1996. DOCUMENT TYPE: Patent CA Section: 28 (Heterocyclic Compounds (More Than One Hetero Atom)) Section cross-reference(s): 1 Substituent dihydrophthalazine compns. are provided which are active as non-NMDA inotropic excitatory amino acid (EAA) receptor antagonists. The compns. are useful for treating disorders assocd. with excessive activation of the non-NMDA subtype of the inotropic EAA receptor. The compds. are useful therapeutically as sedatives or for the treatment of neuropsychopharmacol. disorders such as stroke, ischemia and epilepsy. 186252-59-5 which is the cas registry number of one of substances is just one of reagents here. The compns. may be provided in combination with a suitable carrier for oral or parental administration. The compds. may be administered orally or parenterally for the treatment of a variety of disorders assocd. with non-NMDA EAA receptor function. .