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6-chloro-9-(cyclohex-2-en-1-yl)-9H-purine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

91066-65-8

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91066-65-8 Usage

Properties

Purine core
Chlorine atom at the 6th position
Cyclohexenyl group at the 9th position

Classification

Purine derivative

Uses

Medicinal chemistry, drug development

Pharmacological activities

Antiviral, anticancer, anti-inflammatory

Importance

Valuable building block for synthesis of biologically active molecules

Application

Starting material for creation of new pharmaceutical compounds

Research focus

Important target for research and development in medicinal chemistry.

Check Digit Verification of cas no

The CAS Registry Mumber 91066-65-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,1,0,6 and 6 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 91066-65:
(7*9)+(6*1)+(5*0)+(4*6)+(3*6)+(2*6)+(1*5)=128
128 % 10 = 8
So 91066-65-8 is a valid CAS Registry Number.

91066-65-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 6-chloro-9-cyclohex-2-en-1-ylpurine

1.2 Other means of identification

Product number -
Other names 6-chloro-9-Boc-1-deazapurine

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:91066-65-8 SDS

91066-65-8Relevant academic research and scientific papers

First synthesis of (-)-neplanocin C

Comin, María J.,Rodriguez, Juan B.

, p. 4639 - 4649 (2007/10/03)

(-)-Neplanocin C (4), a minor component of the neplanocin family of antibiotics and a lead drug for the design of several conformationally constrained nucleosides analogues, was enantioselectively synthesized starting from D-ribono-1,4-lactone via a convergent approach in twelve steps. The proton NMR spectrum of 4 was in agreement with the corresponding natural product. Calculated coupling constants obtained from ab initio molecular modeling studies and from previously published X-ray structure of neplanocin C also corresponded to the spectroscopic data. (C) 2000 Elsevier Science Ltd.

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