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1,3,2-Dioxathiolane,4-(1-methylethyl)-,2,2-dioxide,(4S)-(9CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

168141-49-9

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168141-49-9 Usage

Explanation

The molecular formula represents the number of atoms of each element present in a molecule. In this case, the compound has 6 carbon (C), 10 hydrogen (H), 4 oxygen (O), and 1 sulfur (S) atoms.

Explanation

The systematic name is a standardized way of naming chemical compounds based on their structure. It provides information about the functional groups, connectivity, and stereochemistry of the molecule.

Explanation

Dioxathiolane derivatives are a group of organic compounds that contain a dioxathiolane ring. 1,3,2-Dioxathiolane,4-(1-methylethyl)-,2,2-dioxide,(4S)-(9CI) belongs to this class, indicating its structural similarity to other members of the group.

Explanation

The compound is used in various applications within the pharmaceutical and industrial sectors, which may include the synthesis of drugs, intermediates, or other chemical products.

Explanation

As an irritant, the compound can cause harm to the skin, eyes, or respiratory system upon contact or inhalation. It is essential to handle this chemical with care and follow proper safety protocols to minimize the risk of exposure.

Explanation

The stereochemistry of a molecule refers to the spatial arrangement of its atoms. In this case, the (4S)-(9CI) notation indicates the specific configuration of the chiral center at the 4th position in the molecule, which is important for its biological activity and properties.

Explanation

The compound is described as a complex organic molecule, which means it has a relatively large and intricate structure compared to simpler organic compounds. This complexity can contribute to its unique properties and applications.

Class

Dioxathiolane derivatives

Applications

Pharmaceutical and industrial sectors

Hazard

Irritant

Stereochemistry

(4S)-(9CI)

Complexity

Complex organic molecule

Check Digit Verification of cas no

The CAS Registry Mumber 168141-49-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,8,1,4 and 1 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 168141-49:
(8*1)+(7*6)+(6*8)+(5*1)+(4*4)+(3*1)+(2*4)+(1*9)=139
139 % 10 = 9
So 168141-49-9 is a valid CAS Registry Number.

168141-49-9Upstream product

168141-49-9Downstream Products

168141-49-9Relevant academic research and scientific papers

Practical asymmetric syntheses of all four 2,3-methanoleucine stereoisomers

Burgess, Kevin

, p. 2725 - 2728 (1995)

All four stereoisomers of the 2,3-methanoamino acids BOC-E-cyclo-Leu and BOC-Z-cyclo-Leu were prepared from the optically active diol 4 (and its enantiomer) derived from valine. The challenges associated with introduction protected amine functionalities cis to the side chain were overcome by using the vinylogous malonate synthon, dimethyl gluconate.

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