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1034189-07-5

tert-Butyl (2-(4-(((di-tert-butoxyphosphoryl)oxy)methoxy)-3-formylphenyl)-2-hydroxyethyl)(6-(4-phenylbutoxy)hexyl)carbamate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1034189-07-5 Structure

  • Basic information

    1. Product Name: tert-Butyl (2-(4-(((di-tert-butoxyphosphoryl)oxy)methoxy)-3-formylphenyl)-2-hydroxyethyl)(6-(4-phenylbutoxy)hexyl)carbamate
    2. Synonyms:
    3. CAS NO:1034189-07-5
    4. Molecular Formula:
    5. Molecular Weight: 735.896
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1034189-07-5.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: tert-Butyl (2-(4-(((di-tert-butoxyphosphoryl)oxy)methoxy)-3-formylphenyl)-2-hydroxyethyl)(6-(4-phenylbutoxy)hexyl)carbamate(CAS DataBase Reference)
    10. NIST Chemistry Reference: tert-Butyl (2-(4-(((di-tert-butoxyphosphoryl)oxy)methoxy)-3-formylphenyl)-2-hydroxyethyl)(6-(4-phenylbutoxy)hexyl)carbamate(1034189-07-5)
    11. EPA Substance Registry System: tert-Butyl (2-(4-(((di-tert-butoxyphosphoryl)oxy)methoxy)-3-formylphenyl)-2-hydroxyethyl)(6-(4-phenylbutoxy)hexyl)carbamate(1034189-07-5)

  • 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: 1034189-07-5(Hazardous Substances Data)

1034189-07-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1034189-07-5 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,3,4,1,8 and 9 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1034189-07:
(9*1)+(8*0)+(7*3)+(6*4)+(5*1)+(4*8)+(3*9)+(2*0)+(1*7)=125
125 % 10 = 5
So 1034189-07-5 is a valid CAS Registry Number.

1034189-07-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name {2-[4-(di-tert-butoxy-phosphoryloxymethoxy)-3-formyl-phenyl]-2-hydroxy-ethyl}-[6-(4-phenyl-butoxy)-hexyl]-carbamic acid tert-butyl ester

1.2 Other means of identification

Product number -
Other names [2-[4-(Di-tert-butoxyphosphoryloxymethoxy)-3-formylphenyl]-2-hydroxyethyl]-[6-(4-phenylbutoxy)hexyl]carbamic acid tert-butyl 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:1034189-07-5 SDS

1034189-07-5Relevant articles and documents

CORTICOSTEROID LINKED BETA-AGONIST COMPOUNDS FOR USE IN THERAPY

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Page/Page column 51, (2009/12/28)

New chemical entities which comprise corticosteroids and phosphorylated β-agonists for use in therapy and compositions comprising and processes for preparing the same.

MONOPHOSPHATES AS MUTUAL PRODRUGS OF MUSCARINIC RECEPTOR ANTAGONISTS AND B-AGONISTS FOR THE TREATMENT OF COPD AND CHRONIC BRONCHITIS

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Page/Page column 31-32, (2008/12/06)

A mutual prodrug of a MRA and a β-agonist for formulation for delivery by aerosolization to inhibit pulmonary bronchoconstriction is described. The mutual prodrug is preferably formulated in a small volume solution (10-500 μL) dissolved in a quarter norma

MONOPHOSPHATES AS MUTUAL PRODRUGS OF ANTI-INFLAMMATORY SIGNAL TRANSDUCTION MODULATORS (AISTM'S) AND β-AGONISTS FOR THE TREATMENT OF PULMONARY INFLAMMATION AND BRONCHOCONSTRICTION

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Page/Page column 30-31, (2008/12/06)

A mutual prodrug of an AISTM and a β-agonist in formulation for delivery by aerosolization to inhibit pulmonary inflammation and bronchoconstriction is described. The mutual prodrug is preferably formulated in a small volume solution (10-500 μL) dissolved

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