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1-azido-17-iodo-3,6,9,12,15-pentaoxaheptadecane is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

936917-40-7

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936917-40-7 Usage

Explanation

The molecular formula represents the number of atoms of each element present in a molecule of the compound.

Explanation

These functional groups give the compound its unique chemical properties and reactivity.

Explanation

Ether linkages are present in the compound, which are formed by the oxygen atom connecting two carbon atoms.
4. Complex organic compound

Explanation

The compound has a complex structure with multiple functional groups and ether linkages, making it a complex organic molecule.

Explanation

The compound may be used as a reagent or precursor for other compounds in the fields of organic synthesis and chemical research.

Explanation

Due to the presence of azide functional groups, which are known to be explosive and toxic, the compound must be handled and stored with caution.

Explanation

The specific properties and uses of the compound would depend on the user's knowledge and experience in the field of chemistry, as well as the intended application of the compound.

Functional groups

Azide and iodine

Ether linkages

Multiple

Potential applications

Organic synthesis and chemical research

Handling and storage

Careful handling and storage required

Expertise required

Depends on the intended application and expertise of the user

Check Digit Verification of cas no

The CAS Registry Mumber 936917-40-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,3,6,9,1 and 7 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 936917-40:
(8*9)+(7*3)+(6*6)+(5*9)+(4*1)+(3*7)+(2*4)+(1*0)=207
207 % 10 = 7
So 936917-40-7 is a valid CAS Registry Number.

936917-40-7Downstream Products

936917-40-7Relevant articles and documents

Stereoselective synthesis of light-activatable perfluorophenylazide- conjugated carbohydrates for glycoarray fabrication and evaluation of structural effects on protein binding by SPR imaging

Deng, Lingquan,Norberg, Oscar,Uppalapati, Suji,Yan, Mingdi,Ramstroem, Olof

, p. 3188 - 3198 (2011)

A series of light-activatable perfluorophenylazide (PFPA)-conjugated carbohydrate structures have been synthesized and applied to glycoarray fabrication. The glycoconjugates were structurally varied with respect to anomeric attachment, S-, and O-linked carbohydrates, respectively, as well as linker structure and length. Efficient stereoselective synthetic routes were developed, leading to the formation of the PFPA-conjugated structures in good yields over few steps. The use of glycosyl thiols as donors proved especially efficient and provided the final compounds in up to 70% total yield with high anomeric purities. PFPA-based photochemistry was subsequently used to generate carbohydrate arrays on a polymeric surface, and surface plasmon resonance imaging (SPRi) was applied for evaluation of carbohydrate-protein interactions using the plant lectin Concanavalin A (Con A) as a probe. The results indicate better performance and equal efficiency of S- and O-linked structures with intermediate linker length.

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