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(1beta,2beta,3alpha)-1,2-epoxycrinan-3-ol is a naturally occurring organic compound with the molecular formula C10H16O3. It is a sesquiterpene, a type of terpene that consists of three isoprene units. This specific compound is characterized by its unique structure, featuring a 1,2-epoxy group and a hydroxyl group at the 3-position. It is found in various plants and has been identified in essential oils, such as those from the plants Artemisia annua and Juniperus communis. The compound is of interest in the field of natural products chemistry due to its potential biological activities and its role in the synthesis of other natural products.

509-88-6

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509-88-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 509-88-6 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 5,0 and 9 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 509-88:
(5*5)+(4*0)+(3*9)+(2*8)+(1*8)=76
76 % 10 = 6
So 509-88-6 is a valid CAS Registry Number.

509-88-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name Flexinin

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:509-88-6 SDS

509-88-6Downstream Products

509-88-6Relevant academic research and scientific papers

Bioinspired enantioselective synthesis of crinine-type alkaloids: Via iridium-catalyzed asymmetric hydrogenation of enones

Zuo, Xiao-Dong,Guo, Shu-Min,Yang, Rui,Xie, Jian-Hua,Zhou, Qi-Lin

, p. 6202 - 6206 (2017/08/29)

A bioinspired enantioselective synthesis of crinine-type alkaloids has been developed by iridium-catalyzed asymmetric hydrogenation of racemic cycloenones. The method features a biomimetic stereodivergent resolution of the substrates bearing a remote arylated quaternary stereocenter. Using this protocol, 24 crinine-type alkaloids and 8 analogues were synthesized in a concise and rapid way with high yield and high enantioselectivity.

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