1-TERT-BUTOXYCARBONYLAMINO-CYCLOHEXANECARBOXYLIC ACID

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1-TERT-BUTOXYCARBONYLAMINO-CYCLOHEXANECARBOXYLIC ACID Basic information
Product Name:1-TERT-BUTOXYCARBONYLAMINO-CYCLOHEXANECARBOXYLIC ACID
Synonyms:1-{[(tert-butoxy)carbonyl]amino}cyclohexane-1-carboxylic acid;RARECHEM EM WB 0029;N-BOC-AMINOCYCLOHEXYLCARBOXYLIC ACID;N-ALPHA-T-BUTOXYCARBONYL-1-AMINO-CYCLOHEXANECARBOXYLIC ACID;N-ALPHA-T-BOC-1-AMINOCYCLOHEXANE CARBOXYLIC ACID;1-TERT-BUTOXYCARBONYLAMINO-CYCLOHEXANECARBOXYLIC ACID;1-BOC-AMINO-CYCLOHEXANE-1-CARBOXYLIC ACID;1-(BOC-AMINO)CYCLOHEXANECARBOXYLIC ACID
CAS:115951-16-1
MF:C12H21NO4
MW:243.3
EINECS:
Product Categories:Amino Acid Derivatives;Amino Acids and Derivatives
Mol File:115951-16-1.mol
1-TERT-BUTOXYCARBONYLAMINO-CYCLOHEXANECARBOXYLIC ACID Structure
1-TERT-BUTOXYCARBONYLAMINO-CYCLOHEXANECARBOXYLIC ACID Chemical Properties
Melting point 176-178 °C (dec.)
storage temp. Sealed in dry,Room Temperature
form solid
color White
BRN 4189683
Major Applicationpeptide synthesis
InChI1S/C12H21NO4/c1-11(2,3)17-10(16)13-12(9(14)15)7-5-4-6-8-12/h4-8H2,1-3H3,(H,13,16)(H,14,15)
InChIKeyURBHKVWOYIMKNO-UHFFFAOYSA-N
SMILESCC(C)(C)OC(=O)NC1(CCCCC1)C(O)=O
CAS DataBase Reference115951-16-1(CAS DataBase Reference)
Safety Information
WGK Germany 3
HazardClass IRRITANT
HS Code 29225090
Storage Class13 - Non Combustible Solids
MSDS Information
ProviderLanguage
SigmaAldrich English
1-TERT-BUTOXYCARBONYLAMINO-CYCLOHEXANECARBOXYLIC ACID Usage And Synthesis
Chemical PropertiesWhite powder
Usespeptide synthesis
reaction suitabilityreaction type: Boc solid-phase peptide synthesis
Synthesis1-tert-butoxycarbonylamide cyclohexanecarboxylic acid was prepared as follows: sodium hydroxide solution (43 mL, 4 mol/L), THF (40 mL) and 1-aminocyclohexanecarboxylic acid (5.0 g, 34.96 mmol) were added to a round-bottomed flask, and di-tert-butyl dicarbonate (9.13 g, 41.96 mmol) was added to the reaction flask at 0 C. After dropwise addition was complete, the reaction system was After the dropwise addition, the reaction system was stirred at room temperature overnight. Water (100 mL) was added to the reaction system, acidified with hydrochloric acid (50 mL, 1 mol/L), then extracted with ethyl acetate (50 mL2), the organic phases were combined, and the organic phases were washed with saturated brine (100 mL2) and dried with anhydrous sodium sulfate. Filtered, evaporated the solvent under reduced pressure, the crude product was purified by silica gel column chromatography (petroleum ether/ethyl acetate (V/V) = 4/1) to give the white solid title compound 1-tert-butoxycarbonylamide cyclohexanecarboxylic acid (7.3 g, 86%).
1-TERT-BUTOXYCARBONYLAMINO-CYCLOHEXANECARBOXYLIC ACID Preparation Products And Raw materials
Preparation Products(1-Carbamoyl-cyclohexyl)-carbamic acid tert-butyl ester-->N-[1-[[(cyanomethyl)amino]carbonyl]cyclohexyl]-, 1,1-dimethylethyl ester
Tag:1-TERT-BUTOXYCARBONYLAMINO-CYCLOHEXANECARBOXYLIC ACID(115951-16-1) Related Product Information
CIS-2-(TERT-BUTOXYCARBONYLAMINO)-CYCLOHEXANECARBOXYLIC ACID 1-tert-Butoxycarbonylamino-cyclohexanecarboxylic acid TRANS-2-TERT-BUTOXYCARBONYLAMINO-CYCLOHEXANECARBOXYLIC ACID Cyclohexanecarboxylic acid N-BOC-AMINO-(4-HYDROXYCYCLOHEXYL)CARBOXYLIC ACID 8-N-BOC-AMINO-1,4-DIOXA-SPIRO[4.5]DECANE-8-CARBOXYLIC ACID 4-(tert-Butoxycarbonylamino)cyclohexanecarboxylic Acid (cis- and trans- mixture),4-TERT-BUTOXYCARBONYLAMINO-CYCLOHEXANECARBOXYLIC ACID 2-TERT-BUTOXYCARBONYLAMINO-CYCLOHEXANECARBOXYLIC ACID 7-(tert-butoxycarbonyl)-7-azabicyclo[2.2.1]heptane-1-carboxylic acid 3-TERT-BUTOXYCARBONYLAMINO-6,6-DICHLORO-BICYCLO[3.1.0]HEXANE-3-CARBOXYLIC ACID BOC-(4-CIS/TRANS)-1, 1-ACCH(4-CH2OH) BOC-(4-CIS/TRANS)-1, 1-ACCH(4-AMINO-FMOC) cis-1-Amino-4-phenylcyclohexanecarboxylic acid, N-BOC protected BOC-(4-CIS/TRANS)-1, 1-ACCH(4-CH2-NH-FMOC) 1-TERT-BUTOXYCARBONYLAMINO-4-OXO-CYCLOHEXANECARBOXYLIC ACID BOC-CIS-1,4-AMINO-1-CYCLOHEXANE CARBOXYLIC ACID BOC-TRANS-1,4-AMINO-1-CYCLOHEXANE CARBOXYLIC ACID BOC-CIS-1,3-AMINO-1-CYCLOHEXANE CARBOXYLIC ACID