104194-10-7

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• Basic information

  1. Product Name: 1,3-Dioxolan-4-one, 2-(1,1-dimethylethyl)-5-methyl-5-(2-nitroethyl)-, (2R-trans)-
  2. Synonyms: 1,3-Dioxolan-4-one, 2-(1,1-dimethylethyl)-5-methyl-5-(2-nitroethyl)-, (2R-trans)-
  3. CAS NO:104194-10-7
  4. Molecular Formula: C10H17 N O5
  5. Molecular Weight: 0
  6. EINECS: N/A
  7. Product Categories: N/A
  8. Mol File: 104194-10-7.mol
  9. Article Data: 1

• 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: 1,3-Dioxolan-4-one, 2-(1,1-dimethylethyl)-5-methyl-5-(2-nitroethyl)-, (2R-trans)-(CAS DataBase Reference)
  10. NIST Chemistry Reference: 1,3-Dioxolan-4-one, 2-(1,1-dimethylethyl)-5-methyl-5-(2-nitroethyl)-, (2R-trans)-(104194-10-7)
  11. EPA Substance Registry System: 1,3-Dioxolan-4-one, 2-(1,1-dimethylethyl)-5-methyl-5-(2-nitroethyl)-, (2R-trans)-(104194-10-7)

• 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: 104194-10-7(Hazardous Substances Data)

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• 1,3-DIOXOLAN-4-ONE,2-(TERT-BUTYL)-5-METHYL-5-(2-NITROETHYL)-,(2R-TRANS)-

  Cas No: 104194-10-7

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104194-10-7 Usage

General Description

1,3-Dioxolan-4-one, 2-(1,1-dimethylethyl)-5-methyl-5-(2-nitroethyl)-, (2R-trans)- is a chemical compound with the molecular formula C10H17NO4. It is a cyclic organic compound that contains a dioxolanone ring with a 2-tert-butyl-5-methyl substituent and a 5-(2-nitroethyl) group. 1,3-Dioxolan-4-one, 2-(1,1-dimethylethyl)-5-methyl-5-(2-nitroethyl)-, (2R-trans)- is a chiral molecule with a trans configuration at the 2-position, and it is commonly used as a building block in organic synthesis and in the development of pharmaceuticals and agrochemicals. Its unique structure and properties make it a valuable intermediate for the production of a variety of compounds in the chemical industry.

Check Digit Verification of cas no

The CAS Registry Mumber 104194-10-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,4,1,9 and 4 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 104194-10:
(8*1)+(7*0)+(6*4)+(5*1)+(4*9)+(3*4)+(2*1)+(1*0)=87
87 % 10 = 7
So 104194-10-7 is a valid CAS Registry Number.

104194-10-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name	(2R,5S)-2-(tert-Butyl)-5-methyl-5-(2'-nitroethyl)-1,3-dioxolan-4-on

1.2 Other means of identification

Product number	-
Other names	-

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:104194-10-7 SDS

104194-10-7Upstream product

• 3638-64-0 1-nitroethylene 
• 104194-02-7 (2R,5R)-2-(1,1-dimethylethyl)-5-methyl-1,3-dioxolan-4-one 

104194-10-7Downstream Products

• 6236-09-5 (S)-citramalic acid 

104194-10-7Relevant articles and documents

163. Asymmetrische Michael-Additionen Stereoselektive Alkylierung chiraler, nicht racemischer Enolate durch Nitroolefine. Herstellung enantiomerenreiner γ-Aminobuttersaeure- und Bernsteinsaeure-Derivative

Calderari, Giorgio,Seebach, Dieter

, p. 1592 - 1604 (2007/10/02)

Chiral, non-racemic lithium-enolates (E,F,G) of 1,3-dioxolan-4-ones, methyl 1,3-oxazolidin-4-carboxylates, methyl 1,3-oxazolin-4-carboxylates, 1,3-oxazolidin-5-ones, and 1,3-imidazolidin-4-ones derived from (S)-lactic acid (2a), (S)-mandelic acid (2b), and (S)-malic acid (2c), or from (S)-alanine (10), (S)-proline (11), (S)-serine (12), and (S)-threonine (13), are added to nitroolefins.Michael adducts (3-9, 14-18) are formed (40-80percent) with selectivities generally above 90percent ds of one of the four possible stereoisomers.Conversions of these nitroalkylated products furnish the α-branched α-hydroxysuccinic acids 28 and 29, the α-hydroxy-γ-amino acid 25, the α,γ-diamino acid 32, the substituted γ-lactames 19-22, and the pyrrolidine 23.The relative and absolute configuration of the products from dioxolanones and nitropropene are derived by chemical correlation and NOE measurements indicating that the steric course of reaction is to be specified as 1k, ul-1,3.The mechanism is discussed.

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