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Carbonic acid, 2-methoxyethyl 4-nitrophenyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 426264-10-0 Structure
  • Basic information

    1. Product Name: Carbonic acid, 2-methoxyethyl 4-nitrophenyl ester
    2. Synonyms:
    3. CAS NO:426264-10-0
    4. Molecular Formula: C10H11NO6
    5. Molecular Weight: 241.2
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 426264-10-0.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: N/A
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: Carbonic acid, 2-methoxyethyl 4-nitrophenyl ester(CAS DataBase Reference)
    10. NIST Chemistry Reference: Carbonic acid, 2-methoxyethyl 4-nitrophenyl ester(426264-10-0)
    11. EPA Substance Registry System: Carbonic acid, 2-methoxyethyl 4-nitrophenyl ester(426264-10-0)
  • 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: 426264-10-0(Hazardous Substances Data)

426264-10-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 426264-10-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,2,6,2,6 and 4 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 426264-10:
(8*4)+(7*2)+(6*6)+(5*2)+(4*6)+(3*4)+(2*1)+(1*0)=130
130 % 10 = 0
So 426264-10-0 is a valid CAS Registry Number.

426264-10-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-methoxyethyl (4-nitrophenyl) carbonate

1.2 Other means of identification

Product number -
Other names Carbonic acid,2-methoxyethyl 4-nitrophenyl ester

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:426264-10-0 SDS

426264-10-0Downstream Products

426264-10-0Relevant articles and documents

Prodrug compound and application ofprodrug compound in treatment of cancer

-

Paragraph 0185-0186, (2021/03/06)

The present invention provides a compound indicated by a formula (I), pharmaceutically acceptable salts or esters thereof, a pharmaceutical composition of the compound, and application of the compoundand the pharmaceutical composition in the inhibition or regulation of the activity of tyrosine kinase and treating disease symptoms or symptoms including cancer mediated by tyrosine kinase.

PRODRUGS OF THE TYROSINE KINASE INHIBITOR FOR TREATING CANCER

-

Paragraph 00148-00149, (2021/03/05)

There are provided compounds of Formula (I), and pharmaceutically acceptable salts and esters thereof, and pharmaceutical compositions thereof, useful for inhibition or modulation of the activity of tyrosine kinases and treatment of disease states or conditions mediated by tyrosine kinases, including cancers. (I)

PROTEASE INHIBITORS HAVING ENHANCED FEATURES

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Paragraph 0180, (2017/02/28)

Provided herein (among other things) are protease inhibitor compounds having enhanced features, along with methods for administering such compounds. For example, the subject compounds can be administered without concomitant administration of a CYP3A4 inhibitor, have increased therapeutic index and/or increased potency, and are low-resistance inducing in nature.

Synthesis and in vitro human skin penetration of oligo- and polymeric ethylene glycol carbonates of zidovudine and stavudine

N'Da, David D.,Breytenbach, Jaco C.,Breytenbach, J. Wilma

scheme or table, p. 575 - 582 (2011/05/28)

In continuation of studies focusing on the transdermal delivery of antiretroviral (ARV) drugs, the skin permeation ability of synthesized homologous series of both oligomeric and polymeric ethylene glycol (PEG) carbonates of zidovudine (3′-azido-3′-deoxyt

NEW ACETYL COENZYME A CARBOXYLASE (ACC) INHIBITORS AND USES IN TREATMENTS OF OBESITY AND DIABETES MELLITUS - 087

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Page/Page column 238, (2009/07/25)

The present invention relates to Acetyl Coenzyme A Carboxylase (ACC) inhibitors according to formula (I), or an enantiomer thereof, or a pharmaceutically acceptable salt thereof, where R1, R2, R3, R4, R5, E, L, Z and n are as defined herein, to processes for preparing such compounds, to pharmaceutical compositions containing them, to the use of such inhibitors and to methods for th eir therapeutic use, particularly in the treatments of obesity and diabetes mellitus.

PEPTIDIC THROMBIN INHIBITOR COMPOUND

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Page 33, (2010/02/06)

The present invention relates to a novel thrombin inhibitor compound which has a good inhibitory effect against thrombosis and can be orally administered, a process for preparing the same, and to a composition for the therapeutic and/or prophylactic treatment of various diseases associated with thrombin inhibition mechanism, which comprises the same as an active ingredient.

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