Welcome to LookChem.com Sign In|Join Free

CAS

  • or

106334-27-4

2-(2-NITROPROPYL)-1,3-DIOXOLANE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

106334-27-4 Suppliers

Post Buying Request

Recommended suppliersmore

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier
  • 106334-27-4 Structure

  • Basic information

    1. Product Name: 2-(2-NITROPROPYL)-1,3-DIOXOLANE
    2. Synonyms: 2-(2-NITROPROPYL)-1,3-DIOXOLANE;2-(2-nitropropyl)-1,3-dioxolaneappox.
    3. CAS NO:106334-27-4
    4. Molecular Formula: C6H11NO4
    5. Molecular Weight: 161.16
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 106334-27-4.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 2-(2-NITROPROPYL)-1,3-DIOXOLANE(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-(2-NITROPROPYL)-1,3-DIOXOLANE(106334-27-4)
    11. EPA Substance Registry System: 2-(2-NITROPROPYL)-1,3-DIOXOLANE(106334-27-4)

  • 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: 106334-27-4(Hazardous Substances Data)

106334-27-4 Usage

Type of compound

Nitro-substituted cyclic ether

Usage

Solvent, reagent in organic synthesis

Flammability

Flammable

Health hazards

Skin and eye irritation upon contact

Common uses

Manufacture of pharmaceuticals, agrochemicals, and other fine chemicals

Safety precautions

Importance of following proper safety protocols to avoid potential harm.

Check Digit Verification of cas no

The CAS Registry Mumber 106334-27-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,6,3,3 and 4 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 106334-27:
(8*1)+(7*0)+(6*6)+(5*3)+(4*3)+(3*4)+(2*2)+(1*7)=94
94 % 10 = 4
So 106334-27-4 is a valid CAS Registry Number.

106334-27-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(2-NITROPROPYL)-1,3-DIOXOLANE

1.2 Other means of identification

Product number -
Other names 2-(1-PIPERAZINO)NICOTINAMIDE

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:106334-27-4 SDS

106334-27-4Relevant articles and documents

3-NITROBUTANAL - EIN NEUER BAUSTEIN FUR METHYL-VERZWEIGTE ZUCKER

Oehrlein, Reinhold,Jaeger,Volker

, p. 6083 - 6086 (1988)

A concept to assemble branched nitrosugars by Henry reaction of 3-nitrobutanal with aldehydes is outlined, and verified by a short synthesis of unnatural D-evernitrose analogues.

UNSYMMETRICAL CONNECTIVE OLEFINATION BY KORNBLUM NITRO-SYNTHESIS : APPLICATIONS IN PHYTUBERIN CHEMISTRY

Crombie, Leslie,Roughley, Brian S.

, p. 3147 - 3156 (2007/10/02)

Kornblum unsymmetrical olefin synthesis employing radical-anion chain crossed-coupling (light catalysed) of a mono- and a gem-di-nitro-compound, followed by reductive NO2 removal, is examined in the context of a hindered olefin structure required for phytuberin synthesis.Whilst successful for a tetrasubstituted olefin model (for which a Witting approach failed), increasing substitution on the β-position of the mono-nitro component supressed the coupling reaction, presumably for steric reasons.An alternative coupling involving a bromonitrocyclohexane and a mononitroacetal caused symmetrical coupling of the mononitro-component in high yield, rather than a crossed reaction.Reductive elimination (using Na2S/DMF) from either rac.- or meso- 1,2-dinitro-1,2-diphenylethane leads to (E)-stilbene 98percent (E) > probably through a stabilised radical or anion.A convenient preparation of triphenylisoxazoline-N-oxide is reported.

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 106334-27-4