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2102-58-1

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2102-58-1 Usage

General Description

"(1S-trans)-2-methyl-5-(1-methylvinyl)cyclohex-2-en-1-ol" is a chemical compound with the molecular formula C10H16O. It is classified as a cyclohexenol, which is a type of cycloalkenol. The compound is a colorless liquid with a molecular weight of 152.23 g/mol. It is commonly used in the production of fragrances and flavors, as well as in the synthesis of other organic compounds. The presence of a methyl and a vinyl group in the structure gives this compound unique chemical properties, making it useful in various industrial applications.

Check Digit Verification of cas no

The CAS Registry Mumber 2102-58-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,1,0 and 2 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 2102-58:
(6*2)+(5*1)+(4*0)+(3*2)+(2*5)+(1*8)=41
41 % 10 = 1
So 2102-58-1 is a valid CAS Registry Number.
InChI:InChI=1/C10H16O/c1-7(2)9-5-4-8(3)10(11)6-9/h4,9-11H,1,5-6H2,2-3H3/t9-,10+/m1/s1

2102-58-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name (-)-trans-Carveol

1.2 Other means of identification

Product number -
Other names (1R,5R)-2-methyl-5-(prop-1-en-2-yl)cyclohex-2-enol

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:2102-58-1 SDS

2102-58-1Relevant articles and documents

Pauson-Khand Reactions with Concomitant C?O Bond Cleavage for the Preparation of 5,5- 5,6- and 5,7-Bicyclic Ring Systems

Ma, Ding,Hu, Naifeng,Ao, Junli,Zang, Shaoli,Yu, Guo,Liang, Guangxin

supporting information, p. 1887 - 1891 (2021/02/26)

Pauson-Khand reactions (PKR) with concomitant C?O bond cleavage have been developed for construction of 5,5- 5,6- and 5,7-bicyclic ring systems bearing complex stereochemistry. The chemistry generates intermolecular PKR-type products in an absolute regio- and stereochemical control which is hardly achievable through real intermolecular Pauson-Khand reactions. A mechanism for this Pauson-Khand reaction has been proposed based on deuterium labelling experiments. (Figure presented.).

Artificial Light-Harvesting Complexes Enable Rieske Oxygenase Catalyzed Hydroxylations in Non-Photosynthetic cells

Bloh, Jonathan Z.,Burek, Bastien O.,Feyza ?zgen, F.,Kourist, Robert,Runda, Michael E.,Schmidt, Sandy,Wied, Peter

, p. 3982 - 3987 (2020/02/04)

In this study, we coupled a well-established whole-cell system based on E. coli via light-harvesting complexes to Rieske oxygenase (RO)-catalyzed hydroxylations in vivo. Although these enzymes represent very promising biocatalysts, their practical applicability is hampered by their dependency on NAD(P)H as well as their multicomponent nature and intrinsic instability in cell-free systems. In order to explore the boundaries of E. coli as chassis for artificial photosynthesis, and due to the reported instability of ROs, we used these challenging enzymes as a model system. The light-driven approach relies on light-harvesting complexes such as eosin Y, 5(6)-carboxyeosin, and rose bengal and sacrificial electron donors (EDTA, MOPS, and MES) that were easily taken up by the cells. The obtained product formations of up to 1.3 g L?1 and rates of up to 1.6 mm h?1 demonstrate that this is a comparable approach to typical whole-cell transformations in E. coli. The applicability of this photocatalytic synthesis has been demonstrated and represents the first example of a photoinduced RO system.

Chemoselective Luche-Type Reduction of α,β-Unsaturated Ketones by Magnesium Catalysis

Jang, Yoon Kyung,Magre, Marc,Rueping, Magnus

, p. 8349 - 8352 (2019/10/16)

The chemoselective reduction of α,β-unsaturated ketones by use of an economic and readily available Mg catalyst has been developed. Excellent yields for a wide range of ketones have been achieved under mild reaction conditions, short times, and low catalyst loadings (0.2-0.5 mol %).

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