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76610-84-9

Basic Information
CAS No.: 76610-84-9
Name: Cefbuperazone
Article Data: 2
Molecular Structure:
Molecular Structure of 76610-84-9 (Cefbuperazone)
Formula: C22H29N9O9S2
Molecular Weight: 627.659
Synonyms: 5-Thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylicacid,7-[[2-[[(4-ethyl-2,3-dioxo-1-piperazinyl)carbonyl]amino]-3-hydroxy-1-oxobutyl]amino]-7-methoxy-3-[[(1-methyl-1H-tetrazol-5-yl)thio]methyl]-8-oxo-,[6R-[6a,7a,7(2R*,3S*)]]-;Cefbuperazone;
Density: 1.772 g/cm3
Melting Point: 118-120 °C
Appearance: Solid
PSA: 280.09000
LogP: -2.23990
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    Cefbuperazone

    Min.Order: 25 Kilogram

    FOB Price:  USD $ 115.0-170.0

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    Hebei Xixun Trading Co., Ltd. is a company specializing in the production, R&D and sales of chemical products. Our main products include pharmaceutical products,food additives, org

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Specification

The Cefbuperazone, with the CAS registry number 76610-84-9, is also known as Tomiporan. This chemical's molecular formula is C22H29N9O9S2 and molecular weight is 627.65. What's more, its systematic name is (6R,7S)-7-([(2R,3S)-2-[(4-ethyl-2,3-dioxopiperazine-1-carbonyl)amino]-3-hydroxybutanoyl]amino)-7-methoxy-3-[(1-methyltetrazol-5-yl)sulfanylmethyl]-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid. Its classification codes are: (1)Antibacterial; (2)Reproductive Effect. This chemical is a second-generation cephalosporin antibiotic.

Physical properties of Cefbuperazone are: (1)ACD/LogP: -1.547; (2)# of Rule of 5 Violations: 2; (3)ACD/LogD (pH 5.5): -4.35; (4)ACD/LogD (pH 7.4): -5.26; (5)ACD/BCF (pH 5.5): 1.00; (6)ACD/BCF (pH 7.4): 1.00; (7)ACD/KOC (pH 5.5): 1.00; (8)ACD/KOC (pH 7.4): 1.00; (9)#H bond acceptors: 18; (10)#H bond donors: 4; (11)#Freely Rotating Bonds: 11; (12)Polar Surface Area: 280.09 Å2; (13)Index of Refraction: 1.779; (14)Molar Refractivity: 148.456 cm3; (15)Molar Volume: 354.208 cm3; (16)Polarizability: 58.853×10-24cm3; (17)Surface Tension: 82.72 dyne/cm; (18)Density: 1.772 g/cm3.

Preparation: 4-Ethyl-2,3-dioxo-1-piperazine carbonyl chloride reacts with D-Threonine, and then add in 7-APA derivative. Methoxyl is introduced to the seventh place by reacting with Lithium methoxide. The final product is formed through hydrolyzing diphenylmethyl in the presence of trifluoroacetic acid.

You can still convert the following datas into molecular structure:
(1)SMILES: O=C2N1/C(=C(\CS[C@@H]1[C@]2(OC)NC(=O)[C@H](NC(=O)N3C(=O)C(=O)N(CC)CC3)[C@@H](O)C)CSc4nnnn4C)C(=O)O
(2)Std. InChI: InChI=1S/C22H29N9O9S2/c1-5-29-6-7-30(16(35)15(29)34)20(39)23-12(10(2)32)14(33)24-22(40-4)18(38)31-13(17(36)37)11(8-41-19(22)31)9-42-21-25-26-27-28(21)3/h10,12,19,32H,5-9H2,1-4H3,(H,23,39)(H,24,33)(H,36,37)/t10-,12+,19+,22-/m0/s1
(3)Std. InChIKey: SMSRCGPDNDCXFR-CYWZMYCQSA-N