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108536-11-4

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108536-11-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 108536-11-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,8,5,3 and 6 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 108536-11:
(8*1)+(7*0)+(6*8)+(5*5)+(4*3)+(3*6)+(2*1)+(1*1)=114
114 % 10 = 4
So 108536-11-4 is a valid CAS Registry Number.

108536-11-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name [10,13-dimethyl-17-(6-methylheptan-2-yl)-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-yl] (3,4,4-trimethyldioxetan-3-yl)methyl carbonate

1.2 Other means of identification

Product number -
Other names (3beta)-cholest-5-en-3-yl (3,4,4-trimethyl-1,2-dioxetan-3-yl)methyl carbonate

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:108536-11-4 SDS

108536-11-4Downstream Products

108536-11-4Relevant articles and documents

Functionalized 1,2-Dioxetanes as Potential Phototherapeutic Agents: The Synthesis of Carboxylate, Carbonate, Carbamate, and Ether Derivatives of 3-(Hydroxymethyl)-3,4,4-trimethyl-1,2-dioxetane

Adam, Waldemar,Bhushan, Vydia,Fuchs, Rainer,Kirchgaessner, Uwe

, p. 3059 - 3062 (2007/10/02)

With gentle and efficient synthetic methods, 3-(hydroxymethyl)-3,4,4-trimethyl-1,2-dioxetane (1) can be transformed with appropriate electrophiles in moderate to good yields into functionalized derivatives of dioxetane 1.As electrophiles served carboxylic acids, chlorocarbonates, isocyanates, trialkyloxonium salts, and trialkylsilyl chlorides.With 1 these afford respectively dioxetanes with carboxylate, carbonate, carbamate, ether, and silyl ether functionalities.Nucleophilic activation of the hydroxymethyl substituent in the dioxetane 1 can be achieved under mild conditions by pyridine, 4-(dimethylamino)pyridine, potassium hydride, or butyllithium.Such functionalized dioxetanes serve as chemical sources of triplet excited carbonyl compounds which should find interesting utilization in photobiology and photomedicine, e.g. as potential phototherapeutic agents

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