Welcome to LookChem.com Sign In|Join Free

CAS

  • or
Propanedioic acid, [1-(4-methoxyphenyl)-2-[2-nitro-6-(trifluoromethyl)phenyl]ethyl]-, dimethyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

111604-99-0

Post Buying Request

111604-99-0 Suppliers

Recommended suppliersmore

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier
  • Propanedioic acid, [1-(4-methoxyphenyl)-2-[2-nitro-6-(trifluoromethyl)phenyl]ethyl]-, dimethyl ester

    Cas No: 111604-99-0

  • Need to discuss

  • No requirement

  • Adequate

  • Wuhan BJM Pharm Inc.
  • Contact Supplier
  • Propanedioic acid, [1-(4-methoxyphenyl)-2-[2-nitro-6-(trifluoromethyl)phenyl]ethyl]-, dimethyl ester

    Cas No: 111604-99-0

  • Need to discuss

  • No requirement

  • Adequate

  • Weiyel Inc
  • Contact Supplier

111604-99-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 111604-99-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,1,6,0 and 4 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 111604-99:
(8*1)+(7*1)+(6*1)+(5*6)+(4*0)+(3*4)+(2*9)+(1*9)=90
90 % 10 = 0
So 111604-99-0 is a valid CAS Registry Number.

111604-99-0Downstream Products

111604-99-0Relevant articles and documents

Fluoride-catalyzed Michael addition of nitrotoluenes to activated α, β-unsaturated esters

Li, Wen-Sen,Thottathil, John,Murphy, Michael

, p. 6591 - 6594 (2007/10/02)

We have found that in the presence of fluoride ion, nitrotoluenes of type 1 undergo Michael addition to activated α, β-unsaturated esters of type 2 in good to excellent yield (Scheme 1). The generality and limitation of this reaction and its application t

Chemoenzymatic synthesis of benzazepinone calcium channel blocking agents

Das, Jagabandhu,Floyd, David M,Kimball, S David,Patel, Ramesh N,Thottathil, John K

, p. 817 - 820 (2007/10/02)

The synthesis of a 6-trifluoromethyl-benzazepin-2-one derivative (3) from readily available nitro-toluene (4) is described.This synthetic route requires an enantio- and stereo-selective microbial reduction of racemic 13 to form (3R,4S)-cis-alcohol (10).Compound 3 is potent calcium channel blocking agent both in vitro and in vivo.

Benzazepinone calcium channel blockers. 2. Structure-activity and drug metabolism studies leading to potent antihypertensive agents. Comparison with benzothiazepinones

Floyd,Kimball,Krapcho,Das,Turk,Moquin,Lago,Duff,Lee,White,Ridgewell,Moreland,Brittain,Normandin,Hedberg,Cucinotta

, p. 756 - 772 (2007/10/02)

As part of a program to discover potent antihypertensive analogues of diltiazem (3a), we prepared 1-benzazepin-2-ones (4). Benzazepinones competitively displace radiolabeled diltiazem, and show the same absolute stereochemical preferences at the calcium channel receptor protein. Derivatives of 4 containing a trifluoromethyl substituent in the fused aromatic ring show potent and long-acting antihypertensive activity. Studies of the metabolism of 4 lead to the metabolically stable antihypertensive calcium channel blockers 5a and 5c. Benzazepinone 5a is a longer acting and more potent antihypertensive agent than the second generation diltiazem analogue TA-3090 (3e).

Benzazepinone calcium channel blockers. 4. Structure-activity overview and intracellular binding site

Kimball,Floyd,Das,Hunt,Krapcho,Rovnyak,Duff,Lee,Moquin,Turk,Hedberg,Moreland,Brittain,McMullen,Normandin,Cucinotta

, p. 780 - 793 (2007/10/02)

We have synthesized a series of benzazepinones (2) in order to determine the structure-activity relationships (SAR) for calcium channel blockers related to diltiazem. A prerequisite for calcium channel blocking activity in vitro and in vivo is the presenc

Process for benzazepine intermediates

-

, (2008/06/13)

A process is disclosed for providing benzazepine intermediates of the formulae STR1 wherein R3, R4 and Y are as defined herein, which intermediates are useful in a process for the preparation of pharmaceutically useful benzazepine de

4,5-dihydro-1H-benzazepine-3-carboxylic acid esters which are useful as anti-hypertensive agents

-

, (2008/06/13)

Compound of the formula STR1 wherein R3 is aryl and R1 is hydrogen or STR2 are disclosed. These compounds are useful as cardiovascular agents, and especially as anti-hypertensive agents.

Benzazepine derivatives

-

, (2008/06/13)

Vasodilating activity is exhibited by compounds having the formula STR1 and pharmaceutically acceptable salts thereof.

Benzazepine derivatives

-

, (2008/06/13)

Vasodilating activity is exhibited by compounds having the formula STR1 and pharmaceutically acceptable salts thereof.

Post a RFQ

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)

1

What can I do for you?
Get Best Price

Get Best Price for 111604-99-0