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Safety Information

15299

Sigma-Aldrich

Boc-4-Abz-OH

≥98.0% (T)

Synonym(s):

4-(Boc-amino)benzoic acid

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About This Item

Linear Formula:
(CH3)3CO2CNHC6H4CO2H
CAS Number:
66493-39-8
Molecular Weight:
237.25
Beilstein:
2115614
MDL number:
MFCD00037428
UNSPSC Code:
12352209
PubChem Substance ID:
57647354

Assay

≥98.0% (T)

reaction suitability

reaction type: Boc solid-phase peptide synthesis

mp

~200 °C (dec.)

application(s)

peptide synthesis

SMILES string

CC(C)(C)OC(=O)Nc1ccc(cc1)C(O)=O

InChI

1S/C12H15NO4/c1-12(2,3)17-11(16)13-9-6-4-8(5-7-9)10(14)15/h4-7H,1-3H3,(H,13,16)(H,14,15)

InChI key

ZJDBQMWMDZEONW-UHFFFAOYSA-N

Other Notes

BOC-protected derivative of PABA.[1]

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Regulatory Listings

Regulatory Listings are mainly provided for chemical products. Only limited information can be provided here for non-chemical products. No entry means none of the components are listed. It is the user’s obligation to ensure the safe and legal use of the product.

JAN Code

15299-VAR:
15299-BULK:
15299-5G:
15299-1G:
15299-50G:

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Certificates of Analysis (COA)

Lot/Batch Number
BCBG5935V
1209736
13923/1
013923/1
063088/1

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M H Norman et al.
Journal of medicinal chemistry, 39(5), 1172-1188 (1996-03-01)
A series of substituted (4-(4-(1,2-benzisothiazol-3-yl)-1-piperazinyl)butyl)benzamide derivatives was prepared and evaluated as potential atypical antipsychotic agents. The target compounds were readily prepared from their benzoyl chloride, benzoic acid, or isatoic anhydride precursors, and they were evaluated in vitro for their ability

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