C₂₂H₃₉N₇O₅S

Base Information

Chemical Name:C₂₂H₃₉N₇O₅S
CAS No.:1011268-29-3
Molecular Formula:C₂₂H₃₉N₇O₅S
Molecular Weight:513.662
Hs Code.:

C<sub>22</sub>H<sub>39</sub>N<sub>7</sub>O<sub>5</sub>S

Synonyms:

Suppliers and Price of C₂₂H₃₉N₇O₅S

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

BroadPharm
Biotin-PEG2-C6-azide 98%
10 MG
$ 250.00

Total 10 raw suppliers

Chemical Property of C₂₂H₃₉N₇O₅S

Chemical Property:

Purity/Quality:

97% ^*data from raw suppliers

Biotin-PEG2-C6-azide 98% ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Description Biotin-PEG2-C6-azide is PEG linker containing a biotin group and an azide group. The azide group can react with either alkyne moiety in Cu(I)-catalyzed Click Chemistry reaction or DBCO moiety in copper-free Click Chemistry reaction to form a stable triazole linkage. The spacer arm helps to minimize steric hindrance involved with the binding to avidin molecules.

Technology Process of C₂₂H₃₉N₇O₅S

There total 1 articles about C₂₂H₃₉N₇O₅S which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield:

: 5515-02-6
6-azido-hexanoyl chloride

: 138529-46-1
N-(8-amino-3,6-dioxaoctanyl)biotinamide

: 1011268-29-3
C₂₂H₃₉N₇O₅S

Guidance literature:: With triethylamine; In N,N-dimethyl-formamide;
DOI:10.1021/tx700347w

Reference yield:

: 1011268-23-7
C₉H₁₂O₂

: 1011268-29-3
C₂₂H₃₉N₇O₅S

: Ser-Leu-Arg-Arg-Ser-Ser-Cys-Phe-Gly-Gly-Arg

: C₈₀H₁₃₇N₂₇O₂₂S₂

Guidance literature:: C₉H₁₂O₂; Ser-Leu-Arg-Arg-Ser-Ser-Cys-Phe-Gly-Gly-Arg; In phosphate buffer; dimethyl sulfoxide; at 37 ℃; for 1h; pH=7.4;

With sodium tetrahydroborate; In phosphate buffer; dimethyl sulfoxide;

C₂₂H₃₉N₇O₅S; With copper(II) sulfate; sodium L-ascorbate; tris[(1-benzyl-1H-1,2,3-triazol-4yl)methyl]amine; In phosphate buffer; dimethyl sulfoxide; acetonitrile; at 20 ℃; for 1h; Further stages.;
DOI:10.1021/tx700347w

Reference yield:

: 1011268-23-7
C₉H₁₂O₂

: 1011268-29-3
C₂₂H₃₉N₇O₅S

: 107489-37-2
Leu-Glu-Asp-Gly-Pro-Lys-Phe-Leu

: C₇₄H₁₁₈N₁₆O₁₉S

: C₇₄H₁₂₀N₁₆O₂₀S

Guidance literature:: C₉H₁₂O₂; Leu-Glu-Asp-Gly-Pro-Lys-Phe-Leu; In phosphate buffer; dimethyl sulfoxide; at 37 ℃; for 1h; pH=7.4;

With sodium tetrahydroborate; In phosphate buffer; dimethyl sulfoxide;

C₂₂H₃₉N₇O₅S; With copper(II) sulfate; sodium L-ascorbate; tris[(1-benzyl-1H-1,2,3-triazol-4yl)methyl]amine; In phosphate buffer; dimethyl sulfoxide; acetonitrile; at 20 ℃; for 1h; Further stages. Title compound not separated from byproducts.;
DOI:10.1021/tx700347w