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beta-Methyl vinyl phosphate (MAP)

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beta-Methyl vinyl phosphate (MAP) Basic information

Product Name:
beta-Methyl vinyl phosphate (MAP)
Synonyms:
  • p-nitrobenzyl (1r,5r,6s)-6-[(1r)-1-hydroxyethyl]-2-
  • P-NITROBENZYL (1R,5R,6S)-6-[(1R)-1-HYDROXYETHYL]-2-[(DIPHENYLPHOSPHONO)OXY]-1-METHYLCARBAPEN-2-EM-3-CARBOXYLATE
  • P-NITROBENZYL (1R,5R,6S)-6-[(1R)-HYDROXY ETHYL]-2-[(DIPHENYLPHOSPHONO)OXY]-1-METHYL CARBAPEN-2EM-3-CARBOXYLATE
  • 3-(DIPHENOXY-PHOSPHORYLOXY)-6-(1-HYDROXY-ETHYL)-4-METHYL-7-OXO-1-AZA-BICYCLO[3.2.0]HEPT-2-ENE-2-CARBOXYLIC ACID 4-NITRO-BENZYL ESTER
  • (4r,5s,6s)-3-(diphenyloxy)phosphoryloxy-6-[(1r)-1-hydroxyethyl]-4-methyl-7-oxo-1-azabicyclo[3,2,0]hept-2-ene-2-carboxylate
  • 4-NITROBENZYL (1R,5R,6S)-6-[(1R)-1-HYDROXYETHYL]-2-[(DIPHENYLPHOSPHONO)OXY]-1-METHYLCARBAPEN-2-EM-3-CARBOXYLATE
  • 4-NITROBENZYL-(1R,5R,6S)-6-[(1R)-1-HYDROXYETHYL]-2-[(DIPHENYLPHOSPHONO)OXY]-1-METHYLCARBAPEN-2-EM-3-CARBOXYLIC ACID
  • beta-Methyl vinyl phosphate (MAP)
CAS:
90776-59-3
MF:
C29H27N2O10P
MW:
594.51
EINECS:
618-646-2
Product Categories:
  • API intermediates
  • pharmaceutical intermediates
  • other Products
  • Aromatics
  • Chiral Reagents
  • Intermediates & Fine Chemicals
  • Pharmaceuticals
  • Phosphorylating and Phosphitylating Agents
  • bc0001
Mol File:
90776-59-3.mol
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beta-Methyl vinyl phosphate (MAP) Chemical Properties

Melting point:
129-131?C
Boiling point:
722.4±60.0 °C(Predicted)
Density 
1.47±0.1 g/cm3(Predicted)
storage temp. 
Sealed in dry,2-8°C
solubility 
Chloroform (Slightly), Methanol (Slightly)
form 
Solid
pka
14.36±0.20(Predicted)
color 
White to Off-White
InChIKey
STULDTCHQXVRIX-PIYXRGFCSA-N
SMILES
N12[C@@]([H])([C@@H]([C@H](O)C)C1=O)[C@@H](C)C(OP(OC1=CC=CC=C1)(OC1=CC=CC=C1)=O)=C2C(OCC1=CC=C([N+]([O-])=O)C=C1)=O
CAS DataBase Reference
90776-59-3(CAS DataBase Reference)
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beta-Methyl vinyl phosphate (MAP) Usage And Synthesis

Description

A chemical compound.

Uses

Meropenem intermediate. A 1β-methyl carbapenem derivative as antibacterial agent.

Synthesis

104873-15-6

2524-64-3

93711-81-0

General procedure for the synthesis of the compound (CAS: 93711-81-0) from 4-β-methylazabicyclohexyl ketone ester (X) and diphenyl chlorophosphate: a solution of 4-β-methylazabicyclohexyl ketone ester (X) was cooled in an ice bath to -10 to -15 °C, and diisopropylethylamine (14.57 g, 0.113 mol) and diphenyl chlorophosphate were added sequentially, protected by nitrogen gas (27.54 g, 0.102 mol). The reaction mixture was kept stirred at the same temperature for 5 hours until the complete disappearance of compound (X) was confirmed by TLC detection. At the end of the reaction, a large number of white crystals were precipitated from the reaction mixture, after which petroleum ether (300 mL) and 3.5% aqueous sodium dihydrogen phosphate (300 mL) were added to the mixture and the crystals were washed by stirring. After filtration, the filter cake was washed with petroleum ether (100 mL) and water (500 mL) in turn, and after drying, the target product PNB (4R,5S,6S)-3-(diphenoxy)phosphoryloxy-6-[(1R)-1-hydroxyethyl]-4-methyl-7-oxo-1-azabicyclo[3.2.0]hept-2-ene-2-carboxylic acid ester (XI) (49.3 g, yield : 81%; purity: 98%). The physicochemical properties of the product were as follows: [α]D25 = +40~+44° (c = 0.5, methanol); melting point: 125-126°C; IR (KBr) νmax cm-1 : 1780, 1745, 1605; 1H NMR (CDCl3) δ: 1.24 (3H, d), 1.35 (3H, d), 2.38 (1H, d, J = 3.2 Hz), 3.35 (1H, dd), 3.52 (1H, m), 4.26 (1H, dd), 4.30 (1H, m), 5.24-5.41 (2H, ABq), 7.29 (10H, m), 7.58 and 8.18 (2H, d).

storage

-20°C Freezer, Under Inert Atmosphere

References

[1] Patent: WO2007/104219, 2007, A1. Location in patent: Page/Page column 15
[2] Journal of Organic Chemistry, 1992, vol. 57, # 15, p. 4243 - 4249
[3] Journal of Antibiotics, 1998, vol. 51, # 8, p. 757 - 770
[4] Patent: WO2007/31858, 2007, A2. Location in patent: Page/Page column 13
[5] Patent: EP2014666, 2009, A1. Location in patent: Page/Page column 10

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