
CAS 18437-66-6: Carbamic acid, N-(4-chlorophenyl)-, 1,1-dimethylethyl ester
Formula:C11H14ClNO2
InChI:InChI=1S/C11H14ClNO2/c1-11(2,3)15-10(14)13-9-6-4-8(12)5-7-9/h4-7H,1-3H3,(H,13,14)
InChI key:InChIKey=VFEHOBXXLPHSOI-UHFFFAOYSA-N
SMILES:N(C(OC(C)(C)C)=O)C1=CC=C(Cl)C=C1
Synonyms:- (4-Chlorophenyl)carbamic acid tert-butyl ester
- 1,1-Dimethylethyl N-(4-chlorophenyl)carbamate
- Carbamic acid, (4-chlorophenyl)-, 1,1-dimethylethyl ester
- Carbamic acid, N-(4-chlorophenyl)-, 1,1-dimethylethyl ester
- Carbanilic acid, p-chloro-, tert-butyl ester
- N-BOC-4-Chloroaniline
- N-tert-Butoxycarbonyl-4-chloroaniline
- Tert-Butyl (4-Chlorophenyl)Carbamate
- p-Chloro-N-tert-butoxycarbonylaniline
- tert-Butyl 4-chlorophenylcarbamate
- tert-Butyl N-(4-chlorophenyl)carbamate
- See more synonyms
Sort by
Found 4 products.
Tert-Butyl (4-Chlorophenyl)Carbamate
CAS:Tert-Butyl (4-Chlorophenyl)CarbamatePurity:98%Molecular weight:227.69g/molTert-Butyl N-(4-chlorophenyl)carbamate
CAS:Purity:97.0%Color and Shape:SolidMolecular weight:227.690002441406254-Chloro-(N-Boc)aniline
CAS:4-Chloro-(N-Boc)aniline is an organic molecule that is used in the synthesis of quinazolinones. It is a nucleophile that reacts efficiently with amines to form substituted anilines. This reaction can be performed in one step, and the product can be used as a starting material for other reactions. The reaction time is short, and this reagent can be reused up to three times without significant loss of reactivity. 4-Chloro-(N-Boc)aniline was developed as a more efficient method for generating quinazolinones than the traditional method using 2-chloroaniline or 2,4-dichlorobenzoyl chloride. This functional group allows for the synthesis of many different types of molecules, such as immunosuppressants, antihistamines, anticonvulsants, and antibiotics.Formula:C11H14ClNO2Purity:Min. 95%Molecular weight:227.69 g/molN-Boc-4-chloroaniline
CAS:Formula:C11H14ClNO2Purity:98%Color and Shape:SolidMolecular weight:227.6874