1-(4-Bromo-2-chlorophenyl)dihydropyrimidine-2,4(1H,3H)-dione
1-(4-Bromo-2-chlorophenyl)dihydropyrimidine-2,4(1H,3H)-dione
제품 개요
빠른 보기
- 제품군
- PROTAC, E3 Ligands & Proximity-Inducing Building Blocks
- 화학명
- 1-(4-Bromo-2-chlorophenyl)dihydropyrimidine-2,4(1H,3H)-dione
- 분자식
- C10H8BrClN2O2
- 분자량
- 303.54
1-(4-Bromo-2-chlorophenyl)dihydropyrimidine-2,4(1H,3H)-dione is a halogenated dihydropyrimidinedione compound identified by CAS 1517523-15-7.
The verified record matches molecular formula C10H8BrClN2O2, molecular weight 303.54, PubChem CID 79777824, and InChIKey OZMYAHMXEBKCKU-UHFFFAOYSA-N.
Its identifiers are best used for compound matching, structure review, and catalog reconciliation.
식별 정보 및 규격
| Catalog No. | CH57001 |
| CAS No. | 1517523-15-7 |
| Chemical Name | 1-(4-Bromo-2-chlorophenyl)dihydropyrimidine-2,4(1H,3H)-dione |
| Molecular Formula | C10H8BrClN2O2 |
| Molecular Weight | 303.54 |
| PubChem CID | 79777824 |
| IUPAC Name | 1-(4-bromo-2-chlorophenyl)-1,3-diazinane-2,4-dione |
| InChIKey | OZMYAHMXEBKCKU-UHFFFAOYSA-N |
응용 맥락
- Chemical identity reference: supports matching the CAS number, formula, molecular weight, PubChem CID, and InChIKey for CH57001.
- Halogenated heterocycle context: provides a bromo/chloro aryl dihydropyrimidinedione record for research cataloging and structure comparison.
- Catalog data alignment: helps keep the product name, public identifier, and molecular formula consistent across product records.
추가 물질 정보
용도
For catalog matching, 1-(4-Bromo-2-chlorophenyl)dihydropyrimidine-2,4(1H,3H)-dione is checked against CAS 1517523-15-7, formula C10H8BrClN2O2, molecular weight 303.54, PubChem CID 79777824, and InChIKey OZMYAHMXEBKCKU-UHFFFAOYSA-N.
특성
- Dihydropyrimidinedione core bearing a 4-bromo-2-chlorophenyl substituent.
- Halogenated aromatic heterocycle with formula C10H8BrClN2O2.
- CAS and exact-name lookups both resolve to PubChem CID 79777824.
관련 기술 자료
공개 출처
- 1-(4-Bromo-2-chlorophenyl)dihydropyrimidine-2,4(1H,3H)-dione | PubChem CID 79777824
- Catalytic in vivo protein knockdown by small-molecule PROTACs
Nature Chemical Biology, 2015
Product-family technical context
- Structural basis of PROTAC cooperative recognition for selective protein degradation
Nature Chemical Biology, 2017
Product-family technical context
- Structural Basis of PROTAC Cooperative Recognition for Selective Protein Degradation
Nature Chemical Biology, 2017
Product-family technical context
- Direct-to-Biology Accelerates PROTAC Synthesis and the Evaluation of Linker Effects on Permeability and Degradation
ACS Medicinal Chemistry Letters, 2022
Product-family technical context
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