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41789-95-1

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41789-95-1 Usage

Description

3-METHOXY-N-METHYLBENZYLAMINE 97, also known as 3-Methoxy-N-Methylbenzylamine, is an organic compound that serves as an intermediate in the synthesis of various pharmaceuticals. It is a liquid with specific chemical properties that make it a valuable component in the production of certain medications.

Uses

Used in Pharmaceutical Industry:
3-METHOXY-N-METHYLBENZYLAMINE 97 is used as an intermediate in the synthesis of diclofensine hydrochloride for its role in the development of pain-relieving and anti-inflammatory medications. Its chemical properties contribute to the effectiveness and potency of the final product, making it a crucial component in the pharmaceutical industry.

Check Digit Verification of cas no

The CAS Registry Mumber 41789-95-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,1,7,8 and 9 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 41789-95:
(7*4)+(6*1)+(5*7)+(4*8)+(3*9)+(2*9)+(1*5)=151
151 % 10 = 1
So 41789-95-1 is a valid CAS Registry Number.
InChI:InChI=1/C9H13NO/c1-10-7-8-4-3-5-9(6-8)11-2/h3-6,10H,7H2,1-2H3/p+1

41789-95-1 Well-known Company Product Price

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  • Alfa Aesar

  • (H54970)  3-Methoxy-N-methylbenzylamine, 97%   

  • 41789-95-1

  • 1g

  • 421.0CNY

  • Detail
  • Alfa Aesar

  • (H54970)  3-Methoxy-N-methylbenzylamine, 97%   

  • 41789-95-1

  • 5g

  • 1451.0CNY

  • Detail

41789-95-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-Methoxy-N-Methylbenzylamine

1.2 Other means of identification

Product number -
Other names 3-Methoxy-N-methylbenzylamine

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:41789-95-1 SDS

41789-95-1Relevant articles and documents

Enabling Synthesis of Triple Reuptake Inhibitor (+)-BMS-820836, a Potential Therapeutic Agent for the Treatment of Depression

Lobben, Paul C.,Amin, Rasidul,Chen, Bang-Chi,Cui, Wenge,Hu, Min,Isherwood, Matthew,Liu, Shuang,Nacro, Kassoum,Miles, Brandon,Mobele, Bingidimi,Olson, Richard E.,Wang, Bei,Yang, Yuh-Lin,Zhao, Rulin

, p. 44 - 50 (2016/01/30)

Herein, we describe the enabling synthesis of (+)-BMS-820836, a 4,7-disubstituted tetrahydroisoquinoline which was developed as a treatment for a range of neurological diseases, including depression and neurophatic pain. In order to advance the drug candi

CRYSTALLINE FORM OF 6-[(4S)-2-METHYL-4-(2-NAPHTHYL)-1,2,3,4-TETRAHYDROISOQUINOLIN-7-YL]PYRIDAZIN-3-AMINE

-

Paragraph 0072; 0074; 0075, (2014/09/30)

The present disclosure generally relates to a crystalline form of 6-[(4S)-2-methyl-4-(naphthyl)-1,2,3,4-tetrahydroisoquinolin-7-yl]pyridazin-3-amine. The present disclosure also generally relates to pharmaceutical compositions comprising the crystalline form, as well of methods of using a crystalline form in the treatment of depression and other conditions and methods for obtaining such crystalline form.

Synthesis and biological evaluation of urea derivatives as highly potent and selective rho kinase inhibitors

Yin, Yan,Lin, Li,Ruiz, Claudia,Khan, Susan,Cameron, Michael D.,Grant, Wayne,Pocas, Jennifer,Eid, Nibal,Park, Hajeung,Schr?ter, Thomas,Lograsso, Philip V.,Feng, Yangbo

, p. 3568 - 3581 (2013/06/27)

RhoA and its downstream effector ROCK mediate stress fiber formation and cell contraction through their effects on the phosphorylation of myosin light chain (MLC). Inhibition of the RhoA/ROCK pathway has proven to be a promising strategy for several indications such as cardiovascular disease, glaucoma, and inflammatory disease. In 2010, our group reported urea-based ROCK inhibitors as potential antiglaucoma agents. These compounds showed potent IC50 values in enzymatic and cell-based assays and significant intraocular pressure (IOP)-lowering effects in rats (~7 mmHg).(22) To develop more advanced ROCK inhibitors targeting various potential applications (such as myocardial infarction, erectile dysfunction, multiple sclerosis, etc.) in addition to glaucoma, a thorough SAR for this urea-based scaffold was studied. The detailed optimization process, counter-screening, and in vitro and in vivo DMPK studies are discussed. Potent and selective ROCK inhibitors with various in vivo pharmacokinetic properties were discovered.

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