3303-84-2
3303-84-2
Chemical Structure
Boc-β-Ala-OH
- CAS No.: 3303-84-2
- Formula:C8H15NO4
- Molecular Weight:189.21
IUPAC Name: 3-((tert-butoxycarbonyl)amino)propanoic acid
InChIKey: WCFJUSRQHZPVKY-UHFFFAOYSA-N
SMILES: O=C(CCNC(OC(C)(C)C)=O)O
Biological Activity: Boc-β-Ala-OH is an alanine derivative[1].
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Boc-β-Ala-OH | 98.0% | Boc-β-Ala-OH is an alanine derivative. | ||||||||||||||||||||
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Boc-NH-PEG1-CH2COOH | 98.0% | Boc-NH-PEG1-CH2COOH is a PEG-based PROTAC linker that can be used in the synthesis of PROTACs. | ||||||||||||||||||||
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4-tert-Butoxy-4-oxobutanoic acid | 99.69% | 4-tert-Butoxy-4-oxobutanoic acid is a PROTAC linker that can be used in the synthesis of PROTACs. | ||||||||||||||||||||
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Boc-GABA-OH | 99.14% | Boc-GABA-OH is a PROTAC linker which can be used to synthesis UNC6852, an EED-targeted PROTAC. | ||||||||||||||||||||
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Boc-NH-C4-acid | 99.65% | Boc-NH-C4-acid is a PROTAC linker, which belongs to a Alkyl/ether linker. Boc-NH-C4-acid can be used in the synthesis of the compound PROTAC1, and specifically degrades EED, EZH2, and SUZ12 in the PRC2 Complex. | ||||||||||||||||||||
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Methyl 3-((tert-butoxycarbonyl)amino)propanoate | Methyl 3-((tert-butoxycarbonyl)amino)propanoate is a PROTAC linker that can be used in the synthesis of PROTACs. | |||||||||||||||||||||
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Boc-Glycine | 99.89% | Boc-Glycine is a Glycine (HY-Y0966) derivative. | ||||||||||||||||||||
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Boc-Glycine-15N | 98.10% | Boc-Glycine-15N is the 15N labeled Boc-Glycine. | ||||||||||||||||||||
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Boc-Glycine-2-13C | Boc-Glycine-2-13C is a 13C-labeled Boc-Glycine (HY-Y0978). Boc-Glycine is a Glycine (HY-Y0966) derivative. | |||||||||||||||||||||
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Boc-Glycine-13C | Boc-Glycine-13C is a 13C-labeled Boc-Glycine (HY-Y0978). Boc-Glycine is a Glycine (HY-Y0966) derivative. | |||||||||||||||||||||
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Boc-Glycine-13C,15N | Boc-Glycine-13C,15N (N-tert-Butoxycarbonyl-2-aminoacetic acid-13C,15N) is the 13C- and 15N-labeled Boc-Glycine (HY-Y0978). Boc-Glycine is a Glycine (HY-Y0966) derivative. | |||||||||||||||||||||
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