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5-methoxyacetylamino-2,4,6-triiodoisophthalic acid [(2,3-dihydroxy-N-methylpropyl)-(2,3-diacetoxypropyl)]diamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1193076-40-2

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1193076-40-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1193076-40-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,9,3,0,7 and 6 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1193076-40:
(9*1)+(8*1)+(7*9)+(6*3)+(5*0)+(4*7)+(3*6)+(2*4)+(1*0)=152
152 % 10 = 2
So 1193076-40-2 is a valid CAS Registry Number.

1193076-40-2Downstream Products

1193076-40-2Relevant academic research and scientific papers

NOVEL PROCESS FOR PREPARATION OF IOPROMIDE

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Page/Page column 6, (2011/02/26)

The present invention relates to a novel process for preparing iopromide which is used as a contrast agent for X-ray, wherein 5-methoxyacetylamino-2,4,6-triiodoisophthalic acid (2,3-diacetoxypropyl)amide chloride of formula (19) and 5-methoxyacetylamino-2,4,6-triiodoisophthalic acid [(2,3-dihydroxy-N-methylpropyl)-(2,3-diacetoxypropyl)]diamide of formula (20) are introduced as intermediates, by which a bismer by-product generated during the preparation process can be removed even without an additional removal procedure and thus iopromide with high purity can be prepared in high yield.

NOVEL PROCESS FOR PREPARATION OF IOPROMIDE

-

Page/Page column 12, (2009/12/05)

The present invention relates to a novel process for preparing iopromide which is used as a contrast agent for X-ray, wherein 5-methoxyacetylamino-2,4,6-triiodoisophthalic acid (2,3-diacetoxypropyl)amide chloride of formula (19) and 5-methoxyacetylamino-2,4,6-triiodoisophthalic acid [(2,3-dihydroxy-N-methylpropyl)-(2,3-diacetoxypropyl)]diamide of formula (20) are introduced as intermediates, by which a bismer by-product generated during the preparation process can be removed even without an additional removal procedure and thus iopromide with high purity can be prepared in high yield.

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