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Heptanoic acid, 7-iodo-, 1,1-dimethylethyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

54005-76-4

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54005-76-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 54005-76-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,4,0,0 and 5 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 54005-76:
(7*5)+(6*4)+(5*0)+(4*0)+(3*5)+(2*7)+(1*6)=94
94 % 10 = 4
So 54005-76-4 is a valid CAS Registry Number.

54005-76-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name tert-butyl 7-iodoheptanoate

1.2 Other means of identification

Product number -
Other names Heptanoic acid,7-iodo-,1,1-dimethylethyl ester

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:54005-76-4 SDS

54005-76-4Relevant academic research and scientific papers

RAS PROTEIN DEGRADERS, PHARMACEUTICAL COMPOSITIONS THEREOF, AND THEIR THERAPEUTIC APPLICATIONS

-

Paragraph 0195; 0258-0259, (2021/03/19)

Provided herein are RAS protein degraders, e.g., a compound of Formula (I), and pharmaceutical compositions thereof. Also provided herein are methods of their use for treating, preventing, or ameliorating one or more symptoms of a RAS-mediated disorder, disease, or condition.

Synthesis of saturated fatty acids 11C (13C)-labelled in the ω-methyl position

Neu, Henrik,Kihlberg, Tor,Langstroem, Bengt

, p. 509 - 524 (2007/10/03)

A method for the preparation of saturated fatty acids 11C (13C)-labelled in the ω-methyl position is described. A highly reactive zerovalent copper complex was prepared from lithium naphtalenide reduced lithium(2-thienyl)iodocuprate. The labelling precursors were obtained by addition of tert-butyl ω-iodocarboxylates to the organocuprate and these were reacted with [11C]methyl iodide to form 11C-labelled, protected intermediates. The tert-butyl ester protecting group was rapidly removed with trifluoroacetic acid, affording fatty acids 11C-labelled in the ω-methyl position. A solid phase extraction method was developed and preceded final HPLC purification. In a typical run starting with 2.75 GBq of [11C]methyl iodide, 375 MBq (66%) [16-11C]palmitic acid was obtained within 46 min from the end of radionuclide production.

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