199800-49-2

• 

• Basic information

  1. Product Name: AG-041R
  2. Synonyms: AG-041R;AG-041R Exclusive
  3. CAS NO:199800-49-2
  4. Molecular Formula: C31H36N4O5
  5. Molecular Weight: 544.64134
  6. EINECS: N/A
  7. Product Categories: N/A
  8. Mol File: 199800-49-2.mol
  9. Article Data: 9

• Chemical Properties

  1. Melting Point: N/A
  2. Boiling Point: 766.592°C at 760 mmHg
  3. Flash Point: 417.42°C
  4. Appearance: /
  5. Density: 1.259g/cm³
  6. Vapor Pressure: 0mmHg at 25°C
  7. Refractive Index: 1.625
  8. Storage Temp.: N/A
  9. Solubility: N/A
  10. CAS DataBase Reference: AG-041R(CAS DataBase Reference)
  11. NIST Chemistry Reference: AG-041R(199800-49-2)
  12. EPA Substance Registry System: AG-041R(199800-49-2)

• Safety Data

  1. Hazard Codes: N/A
  2. Statements: N/A
  3. Safety Statements: N/A
  4. WGK Germany:
  5. RTECS:
  6. HazardClass: N/A
  7. PackingGroup: N/A
  8. Hazardous Substances Data: 199800-49-2(Hazardous Substances Data)

• Suppliers
• Usage
• SDS
• Upstream product
• Downstream Products
• Article

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199800-49-2 Usage

Uses

AG-041R is a potent gastrin/CCKB receptor antagonist that exhibits selective binding for CCKB compared to CCKA.

Check Digit Verification of cas no

The CAS Registry Mumber 199800-49-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,9,9,8,0 and 0 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 199800-49:
(8*1)+(7*9)+(6*9)+(5*8)+(4*0)+(3*0)+(2*4)+(1*9)=182
182 % 10 = 2
So 199800-49-2 is a valid CAS Registry Number.

InChI:InChI=1/C31H36N4O5/c1-5-39-28(40-6-2)20-35-26-10-8-7-9-25(26)31(29(35)37,19-27(36)32-23-15-11-21(3)12-16-23)34-30(38)33-24-17-13-22(4)14-18-24/h7-18,28H,5-6,19-20H2,1-4H3,(H,32,36)(H2,33,34,38)/t31-/m1/s1

199800-49-2SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name	2-[(3R)-1-(2,2-diethoxyethyl)-3-[(4-methylphenyl)carbamoylamino]-2-oxoindol-3-yl]-N-(4-methylphenyl)acetamide

1.2 Other means of identification

Product number	-
Other names	AG-041R

1.3 Recommended use of the chemical and restrictions on use

Identified uses	For industry use only.
Uses advised against	no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number	-
Service hours	Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:199800-49-2 SDS

199800-49-2Upstream product

• 159884-50-1 [1-(2,2-diethoxy-ethyl)-2-oxo-3-(3-p-tolyl-ureido)-2,3-dihydro-1H-indol-3-yl]-acetic acid 
• 106-49-0 p-toluidine 
• 1188395-65-4 (R)-1-(2,2-diethoxyethyl)-1′-(p-tolyl)-1′H-spiro[indoline-3,4′-pyrimidine]-2,2′,6′(3′H,5′H)-trione 
• 159884-41-0 1-(2,2-diethoxyethyl)indoline-2,3-dione 
• 107976-78-3 1H-indole-2,3-dione 3-(O-methyloxime) 
• 91-56-5 indole-2,3-dione 
• 159883-92-8 [(R)-1-(2,2-diethoxyethyl)-2-oxo-3-(3-p-tolylureido)-2,3-dihydro-1H-indol-3-yl]acetic acid (1R,2S,5R)-2-isopropyl-5-methylcyclohexyl ester 
• 195451-17-3 N-[1-(2,2-diethoxyethyl)-2,3-dihydro-2-oxo-1H-indol-3-yl]-N'-(4-methylphenyl)urea 
• 159884-54-5 1-(2,2-diethoxyethyl)-1H-indole-2,3-dione 3-(O-methyloxime) 

199800-49-2Downstream Products

199800-49-2Relevant articles and documents

Catalytic Enantioselective Decarboxylative Mannich-Type Reaction of N-Unprotected Isatin-Derived Ketimines

Sawa, Masanao,Miyazaki, Shotaro,Yonesaki, Ryohei,Morimoto, Hiroyuki,Ohshima, Takashi

, p. 5393 - 5397 (2018/09/13)

The first catalytic enantioselective decarboxylative Mannich-type reaction of N-unprotected ketimines is reported, directly providing N-unprotected 3-tetrasubstituted 3-aminooxindoles in high yield and ee without protection/deprotection steps. The utility

An asymmetric acetate-Mannich reaction of chiral isatin derived ketimines and its applications

Hajra, Saumen,Bhosale, Suhas Shivajirao,Hazra, Atanu

, p. 9217 - 9225 (2017/11/14)

A highly efficient TMSOTf-mediated asymmetric acetate-Mannich reaction of isatin derived tert-butylsulfinyl ketimines and S-phenyl thioacetate was developed to afford the direct synthesis of indole-based β3,3-amino acid thioester with excellent selectivity (dr > 98 : 2). Syntheses of (+)-AG-041R and 3-aminopyrroloindoline have been accomplished utilizing the developed method.

Enantioselective synthesis of AG-041R by using N-heteroarenesulfonyl cinchona alkaloid amides as organocatalysts

Hara, Noriyuki,Nakamura, Shuichi,Sano, Masahide,Tamura, Ryota,Funahashi, Yasuhiro,Shibata, Norio

, p. 9276 - 9280 (2012/08/28)

The organocatalytic enantioselective decarboxylative addition of malonic acid half thioesters to ketimines derived from isatins by using N-heteroarenesulfonyl cinchona alkaloid amides afforded products with high enantioselectivity. The products could be c

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