ChemAbout
© 2026 ChemAbout
Insights|Privacy Policy|Terms of Service|[email protected]
Home/Compounds/Research Reagent/TL13-112
C49H60ClN9O10S
1002.6 g/mol
Research Reagent

TL13-112

CAS2229037-19-6
Category
Research Reagent
Compound Class
Heterocycle
Primary Use
Research Compound

TL13-112 is a research compound with a complex, flexible structure containing multiple aromatic rings and amide groups. It is primarily used as a laboratory reagent for investigational studies.

Content scope: Information here supports chemical identification and industrial supply, research, and manufacturing contexts. It is not a therapeutic claim, medical advice, or drug-use instructions.

Sourcing or supplying this compound?

List your inventory or post a purchase request

CAS 2229037-19-6

List This Product
Sign in to publish supply information
Request This Product
Submit a request without registering

Related Compounds

SimilarStructure SimilarSimilarity 0.83

2-(4-(4-((5-Chloro-4-((2-(isopropylsulfonyl)phenyl)amino)pyrimidin-2-yl)amino)-5-isopropoxy-2-methylphenyl)piperidin-1-yl)-N-(2-((2-(2,6-dioxopiperidin-3-yl)-1,3-dioxoisoindolin-4-yl)amino)ethyl)acetamide

CAS2229036-62-6

research compound

SimilarStructure SimilarSimilarity 0.77

TL13-12

CAS2229037-04-9

research compound

ReferenceSame Category

1,1-difluoro-2-methyl-3-(oxan-2-yl)propan-2-amine

CAS2229522-47-6

research compound

ReferenceSame Category

(+/-)-alpha-BHC-13C6

CAS222966-66-7

research compound

ReferenceSame Category

4-(6-(tert-butoxy)-3,4-dihydronaphthalen-1-yl)phenol

CAS2229713-85-1

research compound

ReferenceSame Category

1-(4-((1R,2S)-6-hydroxy-2-phenyl-1,2,3,4-tetrahydronaphthalen-1-yl)phenyl)piperidine-4-carbaldehyde

CAS2229714-01-4

research compound

Identifiers
IUPAC Name

N-[2-[2-[2-[4-[4-[[5-chloro-4-(2-propan-2-ylsulfonylanilino)pyrimidin-2-yl]amino]-2-methyl-5-propan-2-yloxyphenyl]piperidin-1-yl]ethoxy]ethoxy]ethyl]-2-[[2-(2,6-dioxopiperidin-3-yl)-1,3-dioxoisoindol-4-yl]amino]acetamide

InChIKey

XIRQUXILNXIWDI-UHFFFAOYSA-N

SMILES

CC1=CC(=C(C=C1C2CCN(CC2)CCOCCOCCNC(=O)CNC3=CC=CC4=C3C(=O)N(C4=O)C5CCC(=O)NC5=O)OC(C)C)NC6=NC=C(C(=N6)NC7=CC=CC=C7S(=O)(=O)C(C)C)Cl

Synonyms (3)
  • TL13-112