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115362-12-4

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115362-12-4 Usage

General Description

(-)-(2S,3S)-2,3-Epoxy-3-cyclohexyl-1-propanol is a chemical compound with a molecular formula C9H16O2. It is a cyclohexane derivative that contains an epoxy functional group, which is a three-membered cyclic ether. (-)-(2S,3S)-2,3-Epoxy-3-cyclohexyl-1-propanol is optically active, meaning it exists in two enantiomeric forms, with the (-)-(2S,3S) form being the one described here. (-)-(2S,3S)-2,3-Epoxy-3-cyclohexyl-1-propanol is a colorless liquid with a mild, sweet odor. It is used in the production of various chemicals and pharmaceuticals, and may also have applications in organic synthesis and research.

Check Digit Verification of cas no

The CAS Registry Mumber 115362-12-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,5,3,6 and 2 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 115362-12:
(8*1)+(7*1)+(6*5)+(5*3)+(4*6)+(3*2)+(2*1)+(1*2)=94
94 % 10 = 4
So 115362-12-4 is a valid CAS Registry Number.
InChI:InChI=1/C9H16O2/c10-6-8-9(11-8)7-4-2-1-3-5-7/h7-10H,1-6H2/t8-,9-/m0/s1

115362-12-4SDS

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 (-)-(2S,3S)-2,3-epoxy-3-cyclohexyl-1-propanol

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:115362-12-4 SDS

115362-12-4Relevant articles and documents

New one-pot procedure for the synthesis of diprotected amino alcohols from unprotected vinyl aziridines

Righi, Giuliana,Bovicelli, Paolo,Tirotta, Ilaria

, p. 6439 - 6442 (2013/11/19)

An unprecedented one-pot reaction that allows the synthesis of diprotected amino alcohols from unprotected vinyl aziridines is reported. The results demonstrate the possibility to use various acyl chlorides in order to obtain differently functionalised fragments. Mechanistic insights are given.

A highly stereoselective synthesis of glycidic amides based on a new class of chiral sulfonium salts: Applications in asymmetric synthesis

Sarabia, Francisco,Vivar-García, Carlos,García-Castro, Miguel,García-Ruiz, Cristina,Martín-Gálvez, Francisca,Sánchez-Ruiz, Antonio,Chammaa, Samy

supporting information, p. 15190 - 15201 (2013/01/15)

A new type of chiral sulfonium salts that are characterized by a bicyclic system has been designed and synthesized from α-amino acids. Their corresponding ylides, which were prepared by basic treatment of the sulfonium salts, reacted smoothly with a broad array of simple and chiral aldehydes to provide trans-epoxy amides in reasonable to very good yields and excellent stereoselectivities (>98 %). The obtained epoxy amides were found to be useful as synthetic building blocks. Thus, they were reduced into their corresponding epoxy alcohols and subjected to oxirane-ring-opening reactions with different types of nucleophiles.

Spirodiketopiperazine-based CCR5 antagonist: Discovery of an antiretroviral drug candidate

Nishizawa, Rena,Nishiyama, Toshihiko,Hisaichi, Katsuya,Minamoto, Chiaki,Matsunaga, Naoki,Takaoka, Yoshikazu,Nakai, Hisao,Jenkinson, Stephen,Kazmierski, Wieslaw M.,Tada, Hideaki,Sagawa, Kenji,Shibayama, Shiro,Fukushima, Daikichi,Maeda, Kenji,Mitsuya, Hiroaki

, p. 1141 - 1145 (2011/04/16)

Following the discovery that hydroxylated derivative 3 (Fig. 1) was one of the oxidative metabolites of the original lead 1, it was found that hydroxylated compound 4 possesses higher in vitro anti-HIV potency than the corresponding non-hydroxylated compo

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