What is the NABUMETONE RELATED COMPOUND A (15 MG) (1-(6-METHOXY-2-NAPHTHYL)-BUT-1-EN-3-ONE)?

NABUMETONE RELATED COMPOUND A (15 MG) (1-(6-METHOXY-2-NAPHTHYL)-BUT-1-EN-3-ONE) is , while it's Molecular Formula is C15H14O2. Dehydro Nabumetone is an impurity in the synthesis of Nabumetone (N200500), an anti-inflammatory. Antibacterial. Nabumetone USP Related Compound A.

What is the CAS number for NABUMETONE RELATED COMPOUND A (15 MG) (1-(6-METHOXY-2-NAPHTHYL)-BUT-1-EN-3-ONE)?

The CAS number of NABUMETONE RELATED COMPOUND A (15 MG) (1-(6-METHOXY-2-NAPHTHYL)-BUT-1-EN-3-ONE) is 127053-22-9.

What is NABUMETONE RELATED COMPOUND A (15 MG) (1-(6-METHOXY-2-NAPHTHYL)-BUT-1-EN-3-ONE) (127053-22-9) used for?

NABUMETONE RELATED COMPOUND A (15 MG) (1-(6-METHOXY-2-NAPHTHYL)-BUT-1-EN-3-ONE) is a chemical compound derived from the synthesis of Nabumetone, which is an anti-inflammatory and analgesic drug. NABUMETONE RELATED COMPOUND A (15 MG) (1-(6-METHOXY-2-NAPHTHYL)-BUT-1-EN-3-ONE) is characterized by its molecular structure that includes a 6-methoxy-2-naphthyl group and a buten-3-one functional group. It is used as an impurity in the synthesis process of Nabumetone and has potential applications in various industries due to its chemical properties.

What is the NABUMETONE RELATED COMPOUND A (15 MG) (1-(6-METHOXY-2-NAPHTHYL)-BUT-1-EN-3-ONE)?

NABUMETONE RELATED COMPOUND A (15 MG) (1-(6-METHOXY-2-NAPHTHYL)-BUT-1-EN-3-ONE) is , while it's Molecular Formula is C15H14O2. Dehydro Nabumetone is an impurity in the synthesis of Nabumetone (N200500), an anti-inflammatory. Antibacterial. Nabumetone USP Related Compound A.

What is the CAS number for NABUMETONE RELATED COMPOUND A (15 MG) (1-(6-METHOXY-2-NAPHTHYL)-BUT-1-EN-3-ONE)?

The CAS number of NABUMETONE RELATED COMPOUND A (15 MG) (1-(6-METHOXY-2-NAPHTHYL)-BUT-1-EN-3-ONE) is 127053-22-9.

What is NABUMETONE RELATED COMPOUND A (15 MG) (1-(6-METHOXY-2-NAPHTHYL)-BUT-1-EN-3-ONE) (127053-22-9) used for?

NABUMETONE RELATED COMPOUND A (15 MG) (1-(6-METHOXY-2-NAPHTHYL)-BUT-1-EN-3-ONE) is a chemical compound derived from the synthesis of Nabumetone, which is an anti-inflammatory and analgesic drug. NABUMETONE RELATED COMPOUND A (15 MG) (1-(6-METHOXY-2-NAPHTHYL)-BUT-1-EN-3-ONE) is characterized by its molecular structure that includes a 6-methoxy-2-naphthyl group and a buten-3-one functional group. It is used as an impurity in the synthesis process of Nabumetone and has potential applications in various industries due to its chemical properties.

(E)-4-(2-methoxynaphthalen-6-yl)but-3-en-2-one

Detailed Information

Product Name:(E)-4-(2-methoxynaphthalen-6-yl)but-3-en-2-one
CasNo.:127053-22-9
MF:C15H14O2
MW:226.275

pd_nature

Purity:99%
pd_boiling:120-121℃ (ethanol )
Packing:
Throughput:

Product Details;

CasNo： 127053-22-9

MF： C15H14O2

Top Quality Chinese Manufacturer supply 127053-22-9 (E)-4-(2-methoxynaphthalen-6-yl)but-3-en-2-one

Molecular Formula:C15H14O2
Molecular Weight:226.275
Melting Point:120-121℃ (ethanol )
Boiling Point:406.2±20.0 °C(Predicted)
PSA：26.30000
Density:1.119±0.06 g/cm3(Predicted)
LogP:3.45060

127053-22-9 Relevant articles

Carbon-Carbon bond cleavage in activation of the prodrug nabumetone

Varfaj, Fatbardha,Zulkifli, Siti N. A.,Park, Hyoung-Goo,Challinor, Victoria L.,De Voss, James J.,De Montellano, Paul R. Ortiz

, p. 828 - 838 (2014)

Carbon-carbon bond cleavage reactions ar...

Process research and structural studies on nabumetone

Prabhakar,Reddy, C. Bakki,Reddy, Ch. Maheedhara,Nageshwar,Devi, A. Sivalakshmi,Babu, J. Moses,Vyas,Sarma,Reddy

, p. 121 - 125 (1999)

A short, simple and economical process f...

An efficient benchtop system for multigram-scale kinetic resolutions using aldolase antibodies

Turner, James M.,Bui, Tommy,Lerner, Richard A.,Barbas III, Carlos F.,List, Benjamin

, p. 2772 - 2774 (2000)

The preparative scale kinetic resolution...

Breaking the Dogma of Aldolase Specificity: Simple Aliphatic Ketones and Aldehydes are Nucleophiles for Fructose-6-phosphate Aldolase

Roldán, Raquel,Sanchez-Moreno, Israel,Scheidt, Thomas,Hélaine, Virgil,Lemaire, Marielle,Parella, Teodor,Clapés, Pere,Fessner, Wolf-Dieter,Guérard-Hélaine, Christine

, p. 5005 - 5009 (2017)

d-Fructose-6-phosphate aldolase (FSA) wa...

Organocatalytic diastereo- And enantioselective oxa-hetero-Diels-Alder reactions of enones with aryl trifluoromethyl ketones for the synthesis of trifluoromethyl-substituted tetrahydropyrans

Pasha, Maira,Tanaka, Fujie

supporting information, p. 9242 - 9250 (2021/11/16)

Tetrahydropyran derivatives are found in...

A CATALYST FOR ONE POT SYNTHESIS OF NABUMETONE AND PROCESS OF PREPARATION THEREOF

-

Page/Page column 2; 13-17, (2020/11/30)

The present invention relates to novel h...

Enantiocomplementary synthesis of γ-nitroketones using designed and evolved carboligases

Garrabou, Xavier,Verez, Rebecca,Hilvert, Donald

supporting information, p. 103 - 106 (2017/05/16)

Artificial enzymes created by computatio...

127053-22-9 Process route

: rac-4-Hydroxy-4-(6-methoxynaphthalen-2-yl)pentan-2-one

: 127053-22-9
4-(6'-methoxy-2'-naphthyl)-3-buten-2-one

: 67-64-1
acetone

: (R)-4-Hydroxy-4-(6-methoxynaphthalen-2-yl)pentan-2-one

Conditions

Conditions	Yield
With phosphate buffered saline; aldolase antibodies 38C₂; In toluene; for 193h;	44%

: 3453-33-6
6-methoxynaphthalene-2-carbaldehyde

: 67-64-1
acetone

: 127053-22-9
4-(6'-methoxy-2'-naphthyl)-3-buten-2-one