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1,3-Dioxane-5-carboxamide,2,2-dimethyl-(9CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

162706-00-5

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162706-00-5 Usage

Structure

A dioxane ring with a carboxamide group and two methyl substituents

Derivative of

Dioxane

Usage

a. Various industries
b. Personal care products
c. Pharmaceuticals
d. Intermediate in the synthesis of other organic compounds

Toxicity

Low acute toxicity

Long-term effects

Under investigation

Precautions

Proper handling and usage due to potential health risks

Health risks

Potential long-term effects, requires proper precautions during handling and use

Check Digit Verification of cas no

The CAS Registry Mumber 162706-00-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,2,7,0 and 6 respectively; the second part has 2 digits, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 162706-00:
(8*1)+(7*6)+(6*2)+(5*7)+(4*0)+(3*6)+(2*0)+(1*0)=115
115 % 10 = 5
So 162706-00-5 is a valid CAS Registry Number.

162706-00-5Downstream Products

162706-00-5Relevant academic research and scientific papers

Process for the preparation of iopamidol and 5-amino-2,2-dialkyl-1,3-dioxanes

-

, (2008/06/13)

A process for the preparation of Iopamidol and 5-amino-2,2-dialkyl-1,3-dioxanes of formula STR1 wherein R and R1 are the same or different and represent a straight or branched C1 and C2 alkyl group or together with the carbon atom to which they are bonded, form a C5 -C6 cycloaliphatic ring; comprising the transformation of a 2,2-dialkyl-1,3-dioxane-5-carboxylic acid ester of formula STR2 wherein R2 represents a straight or branched C1 -C2 alkyl group, a phenyl optionally substituted by nitro groups or a benzyl; by treatment with ammonia into the corresponding amides and the subsequent rearrangement of the latter into the compounds of formula I, by treatment with a hypohalogenite. The resultant ketals may be used as is, or be converted to 2-amino-1,3-propanediol, and reacted with 5-amino-2,4,6-triiodo-isophthalic acid dichloride or, alternatively,L-5-(2-acetoxy-propionylamino)-2,4,6-triido-isophthalic acid dichloride, to produce Iopamidol.

Proces for the preparation of 5-amino-2,2-dialkyl-1,3-dioxanes

-

, (2008/06/13)

A process for the preparation of 5-amino-2,2-dialkyl-1,3-dioxanes of formula wherein R and R1 have the meanings reported in the description, comprising the transformation of a 2,2-dialkyl-1,3-dioxan-5-carboxylic acid ester of formula wherein R2 has the meanings reported in the description into the corresponding amide and the subsequent rearrangement of this latter into the compounds of formula I, is described.

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