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3306-52-3

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3306-52-3 Usage

General Description

The chemical "[1S-(1alpha,2alpha,11balpha)]-1,7,8,11b-tetrahydro-1-hydroxy-2-methoxy-11b-methylcyclopenta[7,8]phenanthro[10,1-bc]furan-3,6,9(2H)-trione" is a complex compound with a cyclopenta[7,8]phenanthro[10,1-bc]furan-3,6,9(2H)-trione core structure. It contains hydroxy and methoxy functional groups, as well as a methyl substituent on the cyclopentane ring. Due to its intricate structure, this chemical could potentially have a wide range of pharmacological and biological properties, and may be of interest for further research and development in the fields of medicine and chemistry.

Check Digit Verification of cas no

The CAS Registry Mumber 3306-52-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,3,0 and 6 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 3306-52:
(6*3)+(5*3)+(4*0)+(3*6)+(2*5)+(1*2)=63
63 % 10 = 3
So 3306-52-3 is a valid CAS Registry Number.

3306-52-3SDS

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 Viridin

1.2 Other means of identification

Product number -
Other names EINECS 221-987-6

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:3306-52-3 SDS

3306-52-3Downstream Products

3306-52-3Relevant articles and documents

Total Synthesis of Viridin and Viridiol

Ji, Yang,Xin, Zhengyuan,He, Haibing,Gao, Shuanhu

supporting information, p. 16208 - 16212 (2019/10/14)

The asymmetric total synthesis of (-)-viridin and (-)-viridiol, antifungal metabolites, was achieved in 17 and 18 steps from a commercially available starting material. An intramolecular [3+2] cycloaddition was applied to an easily available l-ribose derivative in order to construct the highly substituted D ring containing the key chiral cis-triol fragment. Co-catalyzed metal-hydride H atom transfer (MHAT) radical cyclization was utilized to form the C-ring and the all-carbon quaternary center at C-10. This convergent strategy provides a scalable approach to prepare viridin and viridiol for biological studies.

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