ChemicalBook--->CAS DataBase List--->154235-77-5

154235-77-5

154235-77-5 Structure

154235-77-5 Structure
IdentificationBack Directory
[Name]

benzo[d]oxazole-6-carboxylic acid
[CAS]

154235-77-5
[Synonyms]

6-Benzoxazolecarboxylic acid
Benzoxazole-6-carboxylic Acid
benzo[d]oxazole-6-carboxylic acid
1,3-Benzoxazole-6-carboxylic acid
1,3-Benzoxazole-6-carboxylic acid 97%
[Molecular Formula]

C8H5NO3
[MDL Number]

MFCD09954949
[MOL File]

154235-77-5.mol
[Molecular Weight]

163.13
Chemical PropertiesBack Directory
[Melting point ]

280-290 °C (sublm)(Press: 16 Torr)
[Boiling point ]

350.1±15.0 °C(Predicted)
[density ]

1.455±0.06 g/cm3(Predicted)
[storage temp. ]

2-8°C
[form ]

Solid
[pka]

3.60±0.30(Predicted)
[color ]

Light brown to brown
Safety DataBack Directory
[Symbol(GHS) ]


GHS07
[Signal word ]

Warning
[Hazard statements ]

H302+H312+H332-H315-H319-H335
[Precautionary statements ]

P260-P280-P261
[HS Code ]

2934999090
Hazard InformationBack Directory
[Uses]

6-?Benzoxazolecarboxyli?c Acid is a reactant used in the design, synthesis, structure-activity relationship, and in vivo activity of azabicyclic aryl amides as α7 nicotinic acetylcholine receptor agonists.
[in vivo]

Serpin B9-IN-1 (BTCA) inhibits bone metastasis (BM) in multiple tumor metastasis models. Serpin B9-IN-1 (50 mg/kg/d; ip; 14 d) effectively reduced the survival rate and metastasis proportion of metastatic cancer cells in the mouse bone metastasis model with LLC1-BM3 injected into the tail artery (CA)[1].
Serpin B9-IN-1 (300 μg/d; ip; 14 d) effectively delayed the average time to bone metastasis (BM) in the LLC1-BM3 cell group[1].

Animal Model:LLC1-BM3 Bone Metastatic Mouse Model by CA injections[1]
Dosage:50 mg/kg
Administration:ip; followed after cancer cell injection, injection daily for 14 days
Result:Reduced the survival rate and metastasis proportion of metastatic cancer cells
Animal Model:LLC1-BM3-sr-ctrl Model in Mouse[1]
Dosage:300 μg
Administration:ip; once daily for 14 days
Result:Delayed the mean time to occurrence of bone metastasis (BM), and lowered the burden of BM in LLC1-BM3-shSB9 cells group.
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