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ethyl 2-[(3-amino-2,4,6-triiodo-phenyl)methyl]butanoate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

100850-30-4

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100850-30-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 100850-30-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,0,8,5 and 0 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 100850-30:
(8*1)+(7*0)+(6*0)+(5*8)+(4*5)+(3*0)+(2*3)+(1*0)=74
74 % 10 = 4
So 100850-30-4 is a valid CAS Registry Number.
InChI:InChI=1/C13H16I3NO2/c1-3-7(13(18)19-4-2)5-8-9(14)6-10(15)12(17)11(8)16/h6-7H,3-5,17H2,1-2H3

100850-30-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 10, 2017

Revision Date: Aug 10, 2017

1.Identification

1.1 GHS Product identifier

Product name ethyl 2-[(3-amino-2,4,6-triiodophenyl)methyl]butanoate

1.2 Other means of identification

Product number -
Other names (+/-)-iopanoic acid ethyl 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:100850-30-4 SDS

100850-30-4Downstream Products

100850-30-4Relevant academic research and scientific papers

Diagnostic and Therapeutic Potential of Poly(benzyl L-glutamate)

Yang, David J.,Li, Chun,Nikiforow, Sarah,Gretzer, Matthew B.,Kuang, Li-Ren,et al.

, p. 328 - 331 (1994)

Poly(benzyl L-glutamate) (PBLG) microcapsules, prepared by a solvent evaporation technique for intravenous injection, are evaluated for their potential use in diagnostic computed tomographic enhancement of liver images.The smaller microcapsules, 3 μm, lo

CHEMOENZYMATIC SYNTHESIS OF THE ENANTIOMERS OF IOPANOIC ACID

Colombo, M.,Amici, M. De,Micheli, C. De,Pitre, D.,Carrea, G.,Riva, S.

, p. 1021 - 1030 (2007/10/02)

The two enantiomers of Iopanoic acid 1 were prepared in enantiomeric excess higher than 90percent by enzyme-catalyzed hydrolysis of precursors (+/-)-2a and (+/-)-3a, followed by standard chemical transformations.Among the tested enzymes, chymotrypsin and Lipase PS proved to be the most selective catalysts.The stereochemical outcome of the lipase-catalyzed hydrolyses of esters (+/-)-2a-d is strictly dependent upon both the size of the alkyl group attached to the chiral center and the substituent in the aromatic ring.The enantioselectivity of the reactions was evaluated by chiral HPLC and the configurations of the new products were assigned by chemical correlations.

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