Cas 96791-17-2,cis-4-phenyl-3-acetamido-3-carbomethoxy-Δ<sup>1</sup>-pyrazoline

96791-17-2

Post Buying Request

Basic information

Product Name: cis-4-phenyl-3-acetamido-3-carbomethoxy-Δ¹-pyrazoline
Synonyms: cis-4-phenyl-3-acetamido-3-carbomethoxy-Δ¹-pyrazoline
CAS NO:96791-17-2
Molecular Formula:
Molecular Weight: 261.28
EINECS: N/A
Product Categories: N/A

Chemical Properties

Melting Point: N/A
Boiling Point: N/A
Flash Point: N/A
Appearance: N/A
Density: N/A
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: cis-4-phenyl-3-acetamido-3-carbomethoxy-Δ¹-pyrazoline(CAS DataBase Reference)
NIST Chemistry Reference: cis-4-phenyl-3-acetamido-3-carbomethoxy-Δ¹-pyrazoline(96791-17-2)
EPA Substance Registry System: cis-4-phenyl-3-acetamido-3-carbomethoxy-Δ¹-pyrazoline(96791-17-2)

Safety Data

Hazard Codes: N/A
Statements: N/A
Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 96791-17-2(Hazardous Substances Data)

Suppliers
Usage
Upstream product
Downstream Products
Article

96791-17-2 Suppliers

Recommended suppliers

96791-17-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 96791-17-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,6,7,9 and 1 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 96791-17:
(7*9)+(6*6)+(5*7)+(4*9)+(3*1)+(2*1)+(1*7)=182
182 % 10 = 2
So 96791-17-2 is a valid CAS Registry Number.

96791-17-2Upstream product

96791-17-2Downstream Products

96791-17-2Relevant academic research and scientific papers

NEW EFFICIENT SYNTHESIS OF 3(5)-CARBOMETHOXY-4-ARYLPYRAZOLES FROM 3-ARYL-2,3-DEHYDROAMINO ACID DERIVATIVES

Catiela, Carlos,Villegas, M. Dolores Diaz de,Gainza, M. Pilar

, p. 165 - 172 (2007/10/02)

3(5)-Carbomethoxy-4-arylpyrazoles can be easily obtained by aromatization with boron trifluoride etherate of 4-aryl-3-acetamido(or benzamido)-3-carbomethoxy-Δ1-pyrazolines synthesized by 1,3-dipolar cycloaddition of diazomethane with 3-aryl-2,3

Synthesis of Methyl (Z)-2-Acetamido-3-aryl-2-butenoates in Two Highly Selective Steps

Cativiela, C.,Diaz de Villegas, M. D.,Melendez, E.

, p. 418 - 419 (2007/10/02)

Diazomethane reacts with methyl (Z)-2-acetamido-3-aryl-2-propenoates regio- and stereospecifically to afford cis-4-aryl-3-acetamido-3-methoxycarbonyl-Δ1-pyrazolines which heated in 1,2-ethanediol at 200 deg C extrude nitrogen to afford stereospecifically methyl (Z)-2-acetamido-3-aryl-2-butenoates in high yields.

ON THE SYNTHESIS OF METHYL (Z/E)-2-ACETAMIDO(OR BENZAMIDO)-3-ARYL 2-BUTENOATES

Cativiela, C.,Villegas, M. D. Diaz de,Melendez, E.

, p. 583 - 590 (2007/10/02)

The methyl Z-2-acetamido(or benzamido)-3-aryl-2-butenoates (Z-9a-e, Z-10a-e) were obtained by two alternative procedures: stereospecific opening of Z-2-methyl(or phenyl)-4-(α-arylethylidene)-5(4H)-oxazolones (Z-7a-e, Z-8a-e) and stereospecific homologatio

Action of Diazomethane on Methyl (Z(or E))-2-(Acylamino)cinnamates. A New Route to Methyl (Z)-2-(Acylamino)-3-methylcinnamates

Cativiela, Carlos,Villegas, Maria D. Diaz de,Mayoral, Jose A.,Melendez, Enrique

, p. 3167 - 3169 (2007/10/02)

Diazomethane reacts with methyl (Z(or E))-2-acetamido(or benzamido)cinnamates (1,2) to afford regio- and stereospecifically (Z(or E))-4-phenyl-3-acetamido(or benzamido)-3-carbomethoxy-Δ1-pyrazolines (3,4). 3Z and 4Z undergo pyrolysis to afford

Post a RFQ

Cas No.:

Product Name:

Quantity:

Email:

Company name:

Valid Period:

Detailed Requirements:

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

What can I do for you?
Get Best Price

Get Best Price for 96791-17-2