Welcome to LookChem.com Sign In|Join Free

CAS

  • or
CarbaMic acid, N-[2-[[(4-chlorophenyl)Methyl]aMino]ethyl]-, 1,1-diMethylethyl ester is a carboxylic acid ester compound derived from CarbaMic acid and 1,1-diMethylethyl alcohol. It is commonly used as a pharmaceutical intermediate and can be found in various drug formulations. This chemical may also have potential applications in research and development for pharmaceutical products.

335059-94-4

Post Buying Request

335059-94-4 Suppliers

Recommended suppliersmore

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier
  • Carbamic acid, N-[2-[[(4-chlorophenyl)methyl]-amino]ethyl]-, 1,1-dimethylethyl ester

    Cas No: 335059-94-4

  • USD $ 1.9-2.9 / Gram

  • 100 Gram

  • 1000 Metric Ton/Month

  • Chemlyte Solutions
  • Contact Supplier

335059-94-4 Usage

Uses

Used in Pharmaceutical Industry:
CarbaMic acid, N-[2-[[(4-chlorophenyl)Methyl]aMino]ethyl]-, 1,1-diMethylethyl ester is used as a pharmaceutical intermediate for the development and formulation of various drugs. Its unique chemical structure allows it to be a key component in the synthesis of active pharmaceutical ingredients.
Used in Research and Development:
This chemical compound is also used in research and development for pharmaceutical products. Its potential applications in drug discovery and development make it a valuable tool for scientists and researchers working in the field of pharmaceuticals.
It is important to handle and use CarbaMic acid, N-[2-[[(4-chlorophenyl)Methyl]aMino]ethyl]-, 1,1-diMethylethyl ester with care and in accordance with safety procedures to minimize any potential health and environmental risks.

Check Digit Verification of cas no

The CAS Registry Mumber 335059-94-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,3,5,0,5 and 9 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 335059-94:
(8*3)+(7*3)+(6*5)+(5*0)+(4*5)+(3*9)+(2*9)+(1*4)=144
144 % 10 = 4
So 335059-94-4 is a valid CAS Registry Number.

335059-94-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name [2-(4-chlorobenzylamino)ethyl]carbamic acid tert-butyl ester

1.2 Other means of identification

Product number -
Other names tert-butyl 2-(4-chlorobenzylamino)ethylcarbamate

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:335059-94-4 SDS

335059-94-4Relevant articles and documents

Inhibitory effect of novel tetrahydropyrimidine-2(1H)-thiones on melanogenesis

Thanigaimalai,Lee, Ki-Cheul,Bang, Seong-Cheol,Lee, Jee-Hyun,Yun, Cheong-Yong,Roh, Eunmiri,Hwang, Bang-Yeon,Kim, Youngsoo,Jung, Sang-Hun

experimental part, p. 1135 - 1142 (2010/04/24)

The series of imidazoldine-2-thiones 2 and tetrahydropyrimidine-2-thiones 3 were discovered as inhibitor of α-MSH-induced melanin production in melanoma B16 cells. The primary bioassay showed that 1-(4-ethylbenzyl)-tetrahydropyrimidine-2(1H)-thione 3e (>1

PYRIMIDYL CYCLOPENTANES AS AKT PROTEIN KINASE INHIBITORS

-

Page/Page column 37, (2009/03/07)

The present invention provides compounds of Formula I, including tautomers, resolved enantiomers, diastereomers, solvates, metabolites, salts and pharmaceutically acceptable prodrugs thereof. Also provided are methods of using the compounds of this invent

SUBSTITUTED 4-BENZYLOXY-BENZOIC ACID AMIDE DERIVATIVES

-

Page/Page column 21-22, (2010/11/25)

The present invention relates to novel substituted 4-benzyloxy-benzoic acid amide derivatives, processes for their preparation, and their use in medicaments, especially for the prophylaxis and treatment of diseases associated with Cold Menthol Receptor 1 (CMR-1) activity, in particular for the treatment of urological diseases or disorders, such as detrusor overactivity (overactive bladder), urinary incontinence, neurogenic detrusor overactivity (detrusor hyperflexia), idiopathic detrusor overactivity (detrusor instability), benign prostatic hyperplasia, and lower urinary tract symptoms; chronic pain, neuropathic pain, postoperative pain, rheumatoid arthritic pain, neuralgia, neuropathies, algesia, nerve injury, ischaemia, neurodegeneration, stroke, and inflammatory disorders such as asthma and chronic obstructive pulmonary (or airways) disease (COPD).

SUBSTITUTED 2-BENZYLOXY-BENZOIC ACID AMIDE DERIVATIVES TECHNICAL FIELD OF THE INVENTION

-

Page/Page column 27, (2010/11/25)

The present invention relates to novel substituted 2-benzyloxy-benzoic acid amide derivatives, processes for their preparation, and their use in medicaments, especially for the prophylaxis and treatment of diseases associated with Cold Menthol Receptor 1

AKT PROTEIN KINASE INHIBITORS

-

Page/Page column 100-101; 152, (2008/06/13)

The present invention provides compounds, including resolved enantiomers, diastereomers, solvates and pharmaceutically acceptable salts thereof, comprising the Formula: A-L-CR where CR is a cyclical core group, L is a linking group and A is as defined herein. Also provided are methods of using the compounds of this invention as AKT protein kinase inhibitors and for the treatment of hyperproliferative diseases such as cancer.

Arylalkylidene rhodanine with bulky and hydrophobic functional group as selective HCV NS3 protease inhibitor

Sing, Wan Theng,Lee, Cheng Leng,Yeo, Su Ling,Lim, Siew Pheng,Sim, Mui Mui

, p. 91 - 94 (2007/10/03)

Arylalkylidene rhodanines 2(a-d) inhibit HCV NS3 protease at moderate concentrations. They are better inhibitors of other serine proteases such as chymotrypsin and plasmin. However, the selectivity of arylmethylidene rhodanines (8a, 9a) with bulkier and more hydrophobic functional groups increases by 13- and 25-fold towards HCV NS3 protease respectively.

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 335059-94-4