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19-iodocholesterol 3-ethyl ether is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

66277-12-1

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66277-12-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 66277-12-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,6,2,7 and 7 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 66277-12:
(7*6)+(6*6)+(5*2)+(4*7)+(3*7)+(2*1)+(1*2)=141
141 % 10 = 1
So 66277-12-1 is a valid CAS Registry Number.
InChI:InChI=1/C29H49IO/c1-6-31-23-14-17-29(19-30)22(18-23)10-11-24-26-13-12-25(21(4)9-7-8-20(2)3)28(26,5)16-15-27(24)29/h10,20-21,23-27H,6-9,11-19H2,1-5H3/t21-,23+,24+,25-,26+,27+,28-,29-/m1/s1

66277-12-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name (3S,8S,9S,10S,13R,14S,17R)-3-ethoxy-10-(iodomethyl)-13-methyl-17-[(2R)-6-methylheptan-2-yl]-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthrene

1.2 Other means of identification

Product number -
Other names Cholest-5-ene,3-ethoxy-19-iodo-,(3beta)

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:66277-12-1 SDS

66277-12-1Downstream Products

66277-12-1Relevant academic research and scientific papers

3-Ethyl and 3-methyl ethers of 19-iodocholesterol as potential adrenal scanning agents.

Owoyale,Szinai

, p. 133 - 141 (1981)

19-Iodocholesterol-131I, though useful as an adrenal scanning agent, was found to be unstable. However, the substitution of methoxyl and ethoxyl groups for the hydroxyl group in the 3 position rendered these derivatives much more stable in solid form than the parent compound. They showed concentration in the adrenals of dogs similar to that of 19-iodocholesterol itself and therefore may be useful as adrenal scanning agents.

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