Basic information Safety Supplier Related

4-BENZYLOXY-5-METHOXY-2-NITRO-BENZOIC ACID

Basic information Safety Supplier Related

4-BENZYLOXY-5-METHOXY-2-NITRO-BENZOIC ACID Basic information

Product Name:
4-BENZYLOXY-5-METHOXY-2-NITRO-BENZOIC ACID
Synonyms:
  • 2-(Benzyloxy)-5-carboxy-4-nitroansole
  • 5-Methoxy-2-nitro-4-(phenylMethyloxy)benzoic acid
  • 2-(Benzyloxy)-5-carboxy-4-nitroansole, 5-(Benzyloxy)-2-carboxy-4-methoxynitrobenzene
  • Benzoic acid, 5-Methoxy-2-nitro-4-(phenylMethoxy)-
  • 4-Benzyloxy-3-Methoxy-6-nitrobenzoic acid
  • 4-BENZYLOXY-5-METHOXY-2-NITRO-BENZOIC ACID
  • 2-Nitro-4-(benzyloxy)-5-methoxybenzoic acid
  • 2-(Benzyloxy)-5-carboxy-4-nitroansole, 5-(Benzyloxy)-2-carboxy-4-methoxynitroben
CAS:
60547-92-4
MF:
C15H13NO6
MW:
303.27
Product Categories:
  • pharmacetical
Mol File:
60547-92-4.mol
More
Less

4-BENZYLOXY-5-METHOXY-2-NITRO-BENZOIC ACID Chemical Properties

Melting point:
192 °C
Boiling point:
504.4±50.0 °C(Predicted)
Density 
1.362±0.06 g/cm3(Predicted)
storage temp. 
Sealed in dry,Room Temperature
pka
2.34±0.25(Predicted)
Appearance
White to off-white Solid
InChI
InChI=1S/C15H13NO6/c1-21-13-7-11(15(17)18)12(16(19)20)8-14(13)22-9-10-5-3-2-4-6-10/h2-8H,9H2,1H3,(H,17,18)
InChIKey
VTHHRADLOLKTLD-UHFFFAOYSA-N
SMILES
C(O)(=O)C1=CC(OC)=C(OCC2=CC=CC=C2)C=C1[N+]([O-])=O
More
Less

Safety Information

HS Code 
2921490090
More
Less

4-BENZYLOXY-5-METHOXY-2-NITRO-BENZOIC ACID Usage And Synthesis

Uses

4-?(Benzyloxy)?-?5-?methoxy-?2-?nitrobenzoic Acid is a reagent used in the preparation of benzodiazepine-based β-glucoside prodrugs for use in cancer chemotherapy.

Synthesis

2426-84-8

60547-92-4

General procedure for the synthesis of 2-nitro-4-benzyloxy-5-methoxybenzoic acid from 4-(benzyloxy)-5-methoxy-2-nitrobenzaldehyde: 4-(benzyloxy)-5-methoxy-2-nitrobenzaldehyde (20 g, 69.62 mmol) was dissolved in acetone (200 mL), and preheated 10% potassium permanganate solution was added slowly at 30 °C. The reaction mixture was stirred at 50 °C for 2 h and then cooled to room temperature. Subsequently, the mixture was filtered through a diatomaceous earth pad and the filter cake was washed with acetone and a little hot water. The filtrate was concentrated under reduced pressure and cooled to 0°C. The concentrate was acidified to pH 4 with hydrochloric acid, stirred for 30 min and filtered to give a solid product of 2-nitro-4-benzyloxy-5-methoxybenzoic acid (18.5 g, 88% yield). The product was confirmed by NMR hydrogen spectrum (300 MHz, DMSO-d6): δ 13.58 (brs, 1H), 7.70 (s, 1H), 7.46-7.40 (m, 6H), 7.39 (s, 1H), 5.25 (s, 2H), 3.92 (s, 3H). Mass spectrum (ESI+, m/z): 304 [M+H]+.

References

[1] Patent: WO2012/30160, 2012, A2. Location in patent: Page/Page column 50
[2] Patent: WO2017/194960, 2017, A1. Location in patent: Page/Page column 187
[3] Patent: US4950674, 1990, A
[4] Farmaco, Edizione Scientifica, 1977, vol. 32, # 8, p. 579 - 591
[5] Tetrahedron Letters, 1986, vol. 27, # 10, p. 1149 - 1152

4-BENZYLOXY-5-METHOXY-2-NITRO-BENZOIC ACIDSupplier

Weifang Ding Hong Pharmaceutical Technology Co., Ltd. Gold
Tel
18663683121
Email
dhpharm@163.com
AstaTech (Chengdu) Pharma. Co., Ltd. Gold
Tel
15928766785 15928766785
Email
wupengcheng@astatech.cn
SiChuang NanBu Honesty Technology Co., Ltd.
Tel
0838-5675166 15883665058
Email
nbcxkj@126.com
Energy Chemical
Tel
021-021-58432009 400-005-6266
Email
sales8178@energy-chemical.com
Shanghai Harvest Chemical Industrial Co., Ltd.
Tel
021-31038972,31038973 17321035817
Email
sales@harvest-chem.com