undecane

Undecane is a high-purity biochemical reagent widely used in biochemical experiments and drug synthesis research.

Undecane (Standard) is the standard substance of Undecane, and it is applicable for quantitative analysis, quality control, and related research in biochemical experiments. Undecane is a high-purity biochemical reagent widely used in biochemical experiments and drug synthesis research.

N-Boc-undecane-1,11-diamine is an alkane chain featuring terminal amine and Boc-protected amino groups. It serves as a PROTAC linker in PROTAC synthesis and other conjugation applications. The amine group can react with carboxylic acids, activated NHS esters, and carbonyl groups (ketones, aldehydes). The Boc group can be deprotected under mild acidic conditions to yield a free amine.

PIP-C-3-Azaspiro[5.5]undecane-boc serves as a linker for PROTAC. It is utilized in synthesizing the PROTAC SOS1 degrader-10.

2-Methoxyphenyl dihydrouracil-azaspiro[5.5]undecane-C-PIP is an E3 ligase ligand-linker conjugate designed for the synthesis of PROTACSOS1 degrader-10.

tert-Butyl 3,9-diazaspiro[5.5]undecane-3-carboxylate is an intermediate used in the synthesis of various active compounds.

1-(Chloroacetyl)-1,4-diazaspiro[5.5]undecane-3,5-dione ,with CAS No. 923155-67-3, is a fragment molecule that serves as an important scaffold for molecular linking, expansion, and modification. 1-(Chloroacetyl)-1,4-diazaspiro[5.5]undecane-3,5-dione provides a structural basis and research tool for the design and screening of novel drug candidates, and is commonly used in drug discovery, drug synthesis, and related research.

1,7-Dioxaspiro[5.5]undecane is a natural male Drosophila sex pheromone, suitable for biochemical experiments and drug synthesis research.

Undecanedioic acid has been found in parts of human aortas with advanced atherosclerotic lesions associated with intercellular matrix macromolecules and specifically with elastin.

369-Trioxaundecanedioic Acid, a PEG-based PROTAC linker, facilitates PROTAC synthesis[1].

1,1,1,3,10,11-Hexachloroundecane is a polychlorinated alkane (PCA) characterized by an elongated carbon chain.

1-Undecanesulfonic Acid Sodium Salt (Standard) is a reference standard of 1-Undecanesulfonic Acid Sodium Salt intended for quantitative analysis, quality control, and related biochemical research applications.

3,6,9-Trioxaundecane-1,11-diyl-bismethanethiosulfonate is a reagent used in biochemical reactions.

11-Maleimidoundecane-1-carbonyl-1-(t-butyl)carbazate is a reagent used in biochemical reactions.

Carboxy-EG6-undecanethiol is an alkanethiol suitable for self-assembling on gold film substrates. It can selectively capture HbA1c from samples through covalent coupling with 3-aminophenylboronic acid (3-APBA).

Amino-EG6-undecanethiol hydrochloride is a biochemical detection reagent utilized as a linker through amide coupling.

1-Bromoundecane (n-Undecyl bromide) is a chemical reagent characterized by a bromine atom attached along a saturated C11 chain. The bromine can be readily substituted by nucleophilic agents such as alcohols or amines. Additionally, 1-Bromoundecane (n-Undecyl bromide) serves as an intermediate in the synthesis of lipids used in lipid nanoparticles.

Undecanenitrile (Decyl cyanide) is a low molecular weight amine solvent that can serve as a reducing agent in debenzylation reactions.

Undecanedioyl-CoA (Undecanedioyl-coenzyme A) is a derivative of coenzyme A.

Bis-Tos-PEG4 (PROTAC Linker 16) is a PEG-based linker utilized in the synthesis of PROTACs.

Tridecanedioic acid (Brassilic acid) is an unusual odd-numbered dicarboxylic acid that appears in the urines of children with neonatal adrenoleukodystrophy and Zellweger syndrome, as an additional marker of these peroxisomal disorders.

CW-3308 is an orally active PROTAC that targets BRD9. It is composed of the PROTAC target protein ligand Naphthyridin-Me-dimethoxybenzene-COOH, the linker 3-Azaspiro[5.5]undecane-9-methanol, and the E3 ubiquitin ligase ligand Thalidomide-methylpyrrolidine. The coupling of the E3 ubiquitin ligase ligand with the linker results in the conjugate Thalidomide-pyrrolidine-C-azaspiro.