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Ethanone, 1-[(1S,3R)-3-(hydroxymethyl)-2,2-dimethylcyclobutyl](9CI) is a complex chemical compound characterized by a cyclobutyl ring with a ketone group and a hydroxymethyl functional group. Its unique stereochemistry and the presence of bulky methyl groups contribute to its distinctive properties, making it a potential candidate for pharmaceutical research and organic synthesis.

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  • Ethanone, 1-[(1S,3R)-3-(hydroxymethyl)-2,2-dimethylcyclobutyl]- (9CI)

    Cas No: 126892-32-8

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  • 126892-32-8 Structure
  • Basic information

    1. Product Name: Ethanone, 1-[(1S,3R)-3-(hydroxymethyl)-2,2-dimethylcyclobutyl]- (9CI)
    2. Synonyms: Ethanone, 1-[(1S,3R)-3-(hydroxymethyl)-2,2-dimethylcyclobutyl]- (9CI)
    3. CAS NO:126892-32-8
    4. Molecular Formula: C9H16O2
    5. Molecular Weight: 156.22214
    6. EINECS: N/A
    7. Product Categories: ACETYLGROUP
    8. Mol File: 126892-32-8.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: Ethanone, 1-[(1S,3R)-3-(hydroxymethyl)-2,2-dimethylcyclobutyl]- (9CI)(CAS DataBase Reference)
    10. NIST Chemistry Reference: Ethanone, 1-[(1S,3R)-3-(hydroxymethyl)-2,2-dimethylcyclobutyl]- (9CI)(126892-32-8)
    11. EPA Substance Registry System: Ethanone, 1-[(1S,3R)-3-(hydroxymethyl)-2,2-dimethylcyclobutyl]- (9CI)(126892-32-8)
  • 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: 126892-32-8(Hazardous Substances Data)

126892-32-8 Usage

Uses

Used in Pharmaceutical Research:
Ethanone, 1-[(1S,3R)-3-(hydroxymethyl)-2,2-dimethylcyclobutyl](9CI) is used as a research compound for exploring its potential applications in the development of new pharmaceuticals. Its unique structure and properties may offer novel therapeutic opportunities.
Used in Organic Synthesis:
Ethanone, 1-[(1S,3R)-3-(hydroxymethyl)-2,2-dimethylcyclobutyl](9CI) is used as a building block in organic synthesis, providing a versatile starting material for the creation of various complex organic molecules. Its unique structure and reactivity can be leveraged to synthesize new compounds with potential applications in various fields.
Further research is required to fully understand the characteristics and potential applications of Ethanone, 1-[(1S,3R)-3-(hydroxymethyl)-2,2-dimethylcyclobutyl](9CI), as its complex structure and unique properties may unlock new possibilities in various industries.

Check Digit Verification of cas no

The CAS Registry Mumber 126892-32-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,6,8,9 and 2 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 126892-32:
(8*1)+(7*2)+(6*6)+(5*8)+(4*9)+(3*2)+(2*3)+(1*2)=148
148 % 10 = 8
So 126892-32-8 is a valid CAS Registry Number.

126892-32-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-((1S,3R)-3-Hydroxymethyl-2,2-dimethyl-cyclobutyl)-ethanone

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:126892-32-8 SDS

126892-32-8Downstream Products

126892-32-8Relevant articles and documents

Selective reduction of aldehydes via BINOL-Zr complex

Lorca, Miguel,Kuhn, Dan,Kurosu, Michio

, p. 6243 - 6246 (2007/10/03)

An easily assembled catalyst from (±)-BINOL (1,1′-bi-naphthol) and Zr(OiPr)4·iPrOH selectively reduces aldehydes at room temperature. Ketones remain intact under these conditions. A catalytic amount of BINOL-Zr complex in the presence of 2-propanol also effectively reduces a variety of chiral and achiral aldehydes.

RADICAL CHEMISTRY BASED ON (+)-CIS-PINONIC ACID

Barton, Derek H. R.,Ozbalik, Nubar,Schmitt, Martine

, p. 3263 - 3266 (2007/10/02)

The capture of the radical from decarboxylation of (+)-cis-pinonic acid has been investigated.Efficient trapping agents give good yields of desired products.Less efficient trapping conditions permit undesired opening of the four-membered ring.

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