Detail of "4389-50-8"

CAS Number:
4389-50-8
Name:
Benzoic acid,2-amino-6-methyl-
Superlist Name:
2-Amino-6-methylbenzoic acid
Molecular Structure:
Formula:
C₈H₉NO₂
Molecular Weight:
151.16
Synonyms:
o-Toluicacid, 6-amino- (6CI,8CI);6-Amino-o-toluic acid;6-Methyl-2-aminobenzoic acid;6-Methylanthranilic acid;ACR 1308;
Density:
1.254 g/cm³
Melting Point:
128-130 °C (dec.)(lit.)
Boiling Point:
315.1 °C at 760 mmHg
Flash Point:
144.4 °C
Appearance:
Pale yellow powder
Hazard Symbols:
Xi
Risk Codes:
36/37/38
Safety:
26-36-24/25 Details

Supplier Location
Supplier Location
- China (Mainland)(14)
- India(3)
- United States(2)
- Japan(1)
Business Type
Business Type
- Lab/Research institutions(2)
- Manufacturers(1)
- Trading Company(14)
Certificates
Certificates
- ISO(2)
- Production License(1)

Display：

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

Herbicidal activity of 6-methylanthranilic acid and analogs: Herbicidal activity of 6-methylanthranilic acid and analogs. Thomas, Gareth J. (Roche Prod. Ltd., Welwyn Garden City AL7 3AY, UK). J. Agric. Food Chem.There are some reagents like 90321-37-2 is used in this study., 32(4), 747-9 (English) 1984. CODEN: JAFCAU. ISSN: 0021-8561. DOCUMENT TYPE: Journal CA Section: 5 (Agrochemical Bioregulators) Analogs of 6-methylanthranilic acid (I) [4389-50-8] were synthesized and their herbicidal activities detd. to define structure-activity relationships. Isomers of I in which carboxyl and amino functions are not ortho were inactive, and anthranilic acids that lack a 6-substituent were considerably less active than I. For optimum activity the 6-substituent should have a lipophilicity parameter p = 0.7 and should be electron donating. Analogs of I with a modified carboxyl function were considerably less active, whereas high activity was retained in a series of N-alkyl and N-acyl derivs. Introduction of addnl. substituents gives analogs with greatly reduced activity. .

Cyclic amine derivatives of substituted quinoxaline 2,3-diones as glutamate receptor antagonists: Cyclic amine derivatives of substituted quinoxaline 2,3-diones as glutamate receptor antagonists. Kornberg, Brian Edward; Nikam, Sham; Rafferty, Michael Francis; Yuen, Po-Wai (Warner-Lambert Company, USA). PCT Int. Appl. WO 9640650 A1 19 Dec 1996, 69 pp.Chemicals with cas numbers 186267-74-3 and 4389-50-8 also play role. DESIGNATED STATES: W: AU, BG, CA, CN, CZ, EE, GE, HU, JP, KR, LT, LV, MX, NO, NZ, PL, RO, SG, SI, SK, UA, UZ, AM, AZ, BY, KG, KZ, MD, RU, TJ, TM; 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: C07D241-44. ICS: C07D401-06. APPLICATION: WO 1996-US6817 13 May 1996. PRIORITY: US 1995-474877 7 Jun 1995. DOCUMENT TYPE: Patent CA Section: 28 (Heterocyclic Compounds (More Than One Hetero Atom)) Title quinoxaline-2,3-diones I (R = cyclic amines, e.g., pyrrolidino, substituted piperidino, morpholino), useful as neuroprotective agents (data), were prepd. by conventional routes via nitroanilines II. Thus, morpholinoaniline II (R = morpholino) was prepd. in three steps from the corresponding benzyl alc., then hydrogenated and cyclized by di-Me oxalate to give the quinoxalinedione which was further nitrated to give I (R = morpholino). .