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138768-04-4

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138768-04-4 Usage

Explanation

Different sources of media describe the Explanation of 138768-04-4 differently. You can refer to the following data:
1. The molecular formula represents the number of atoms of each element present in a molecule. In this case, the compound has 9 carbon (C) atoms, 14 hydrogen (H) atoms, and 2 oxygen (O) atoms.
2. Cyclopentane Derivative
2. The compound is derived from cyclopentane, a five-membered ring of carbon atoms. This indicates its structural similarity to cyclopentane.
3. Contains Ethynyl Group
3. The compound has an ethynyl group (C≡CH), which is a triple-bonded carbon-hydrogen group. This group contributes to the compound's reactivity and properties.
4. Contains Methyl Group
4. The compound also has a methyl group (CH3), which is a single carbon atom bonded to three hydrogen atoms. This group is commonly found in organic compounds and can influence the compound's properties.
5. The stereochemistry of the compound is defined by the (1alpha,2alpha,3alpha) notation, which indicates the spatial arrangement of the atoms in the molecule. This can affect the compound's reactivity and biological activity.
6. Potential Pharmaceutical Applications
6. The compound may have potential uses in the pharmaceutical industry, particularly in drug discovery and development. Its specific applications would depend on its biological activity and pharmacological properties.
7. Industrial Applications
7. The compound may also have industrial applications, such as in the production of specialty chemicals and materials. The specific applications would depend on the compound's chemical properties and reactivity.
8. Further Research and Testing Required
8. To fully understand the properties and potential uses of 1,3-Cyclopentanediol, 2-ethynyl-2-methyl-, (1alpha,2alpha,3alpha)(9CI), additional research and testing are needed. This includes studying its chemical reactivity, stability, and potential interactions with other compounds or biological systems.

Stereochemistry

(1alpha,2alpha,3alpha)

Check Digit Verification of cas no

The CAS Registry Mumber 138768-04-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,8,7,6 and 8 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 138768-04:
(8*1)+(7*3)+(6*8)+(5*7)+(4*6)+(3*8)+(2*0)+(1*4)=164
164 % 10 = 4
So 138768-04-4 is a valid CAS Registry Number.

138768-04-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name (1S,2S,3R)-2-Ethynyl-2-methyl-cyclopentane-1,3-diol

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:138768-04-4 SDS

138768-04-4Downstream Products

138768-04-4Relevant articles and documents

A Catalytic Asymmetric Synthesis of α-Methylene Lactones by the Palladium-catalysed Carbonylation of Prochiral Alkenyl Halides

Suzuki, Takeyuki,Uozumi, Yasuhiro,Shibasaki, Masakatsu

, p. 1593 - 1595 (2007/10/02)

A catalytic asymmetric synthesis of the α-methylene lactones starting with the prochiral alkenyl halides 8 and 19 has been achieved for the first time, giving 9 in 57percent enantiomeric excess (e.e.) and 20 in 39percent e.e., respectively.

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