FMOC-D-PIPECOLIC ACID

Product Name: FMOC-D-PIPECOLIC ACID
CAS No.: 105751-19-7
Chemical Name: FMOC-D-PIPECOLIC ACID
Synonyms: FMOC-D-PIP-OH;FMOC-D-HOPRO-OH;FMOC-D-PIC(2)-OH;FMOC-D-HOMOPRO-OH;FMOC-D-HOMOPROLINE;RARECHEM AR PA 0006;DL-Fmoc-pipecolic acid;D-1-CBZ-PIPECOLINIC ACID;N-Fmoc-DL-pipecolic acid;FMOC-(R)-PIPECOLINIC ACID
CBNumber: CB8186687
Molecular Formula: C21H21NO4
Formula Weight: 351.4
MOL File: 105751-19-7.mol

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FMOC-D-PIPECOLIC ACID Property

Melting point:: 150-151℃
storage temp.: 2-8°C
CAS DataBase Reference: 105751-19-7(CAS DataBase Reference)

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Safety

Hazard Codes: Xi,N
Risk Statements: 36/37/38-50/53
Safety Statements: 26-36-61-60
RIDADR: UN 3077 9/PG 3
WGK Germany: 3
HazardClass: IRRITANT
HazardClass: 9
HS Code: 2933399990

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Hazard and Precautionary Statements (GHS)

Symbol(GHS)
Signal word: Warning
Hazard statements: H400Very toxic to aquatic life
Precautionary statements: P273Avoid release to the environment.

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N-Bromosuccinimide Price

Sigma-Aldrich

Product number: 706477
Product name: N-Fmoc-piperidine-2-carboxylic acid
Purity: 97%
Packaging: 1g
Price: $38.3
Updated: 2023/06/20

Sigma-Aldrich

Product number: 706477
Product name: N-Fmoc-piperidine-2-carboxylic acid
Purity: 97%
Packaging: 5g
Price: $123
Updated: 2023/06/20

Alfa Aesar

Product number: H57178
Product name: N-Fmoc-DL-pipecolic acid, 96+%
Packaging: 1g
Price: $28.98
Updated: 2023/01/06

Alfa Aesar

Product number: H57178
Product name: N-Fmoc-DL-pipecolic acid, 96+%
Packaging: 5g
Price: $113.4
Updated: 2023/01/06

Matrix Scientific

Product number: 042405
Product name: Fmoc-(RS)-piperidine-2-carboxylic acid
Packaging: 1g
Price: $146
Updated: 2021/12/16

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FMOC-D-PIPECOLIC ACID Chemical Properties,Usage,Production

Uses

Reactant for racemic solid-phase preparation of human protease activated receptor 2 agonists and antagonists

Analyte for urea-linked cinchona-calexarene hybrid type receptors for chromatographic enantiomer separation of carbamate-protected amino acids

Combinatorial reactant for assembly of alkylglycine library arrays by SPOT technique on cellulose membranes for identification of micromolar ligands for monoclonal antibodies

FMOC-D-PIPECOLIC ACID Preparation Products And Raw materials

Raw materials

Preparation Products

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FMOC-D-PIPECOLIC ACID Suppliers

Belgium 1 China 47 France 1 Germany 4 India 1 Japan 2 Switzerland 2 United Kingdom 4 United States 16 Global 78

J & K SCIENTIFIC LTD.

Tel: 010-82848833 400-666-7788
Fax: 86-10-82849933
Email: jkinfo@jkchemical.com
Country: China
ProdList: 96815
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Meryer (Shanghai) Chemical Technology Co., Ltd.

Tel: 021-61259108 18621169109
Fax: 86-21-61259102
Email: market03@meryer.com
Country: China
ProdList: 40228
Advantage: 62

Alfa Aesar

Tel: 400-6106006
Fax: 021-67582001/03/05
Email: saleschina@alfa-asia.com
Country: China
ProdList: 30123
Advantage: 84

Energy Chemical

Tel: 021-021-58432009 400-005-6266
Fax: 021-58436166
Email: sales8178@energy-chemical.com
Country: China
ProdList: 44689
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Wuhan Chemwish Technology Co., Ltd

Tel: 86-027-67849912
Fax: 86-027-87531808
Email: sales@chemwish.com
Country: China
ProdList: 35896
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Shanghai Sinch Parmaceuticals Tech. Co. Ltd.

Tel: +86-21-54098501
Fax: +86-21-54096319
Email: sales@sinch.com.cn
Country: China
ProdList: 11598
Advantage: 64

Adamas Reagent, Ltd.

Tel: 400-6009262 16621234537
Fax: 021-64823266
Email: chenyj@titansci.com
Country: China
ProdList: 14103
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Nanjing Chemlin Chemical Co., Ltd

Tel: 025-83697070
Fax: +86-25-83453306
Email: info@chemlin.com.cn
Country: China
ProdList: 19173
Advantage: 64

Shanghai Hanhong Scientific Co.,Ltd.

Tel: 021-54306202 13764082696
Email: info@hanhongsci.com
Country: China
ProdList: 42958
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Candia Thamtech Company Limited

Tel: 0371-86615086 18203638366 0371-86159066 13526786601
Fax: 0371-86159066
Country: China
ProdList: 2015
Advantage: 60

105751-19-7, FMOC-D-PIPECOLIC ACIDRelated Search:

FMOC-D-PIPECOLIC ACID (R)-N-Fmoc-piperidine-2-carboxylic acid, N-Fmoc-D-pipecolic acid,N-ALPHA-FMOC-D-PIPECOLIC ACID,FMOC-D-PIPECOLIC ACID,FMOC-D-(+)-PIPECOLIC ACID FMOC-L-PIPECOLIC ACID,N-ALPHA-FMOC-L-PIPECOLIC ACID,FMOC-L-(-)-PIPECOLIC ACID FMOC-TRANS-3-AZABICYCLO[3.1.0]HEXANE-2-CARBOXYLIC ACID (2S,4R)-FMOC-4-HYDROXYPIPERIDINE-2-CARBOXYLIC ACID (2R,4S)-FMOC-4-HYDROXYPIPERIDINE-2-CARBOXYLIC ACID FMOC-(R,S)-3,4-CIS-METHANOPROLINE FMOC-L-HOMOPRO(4-OXO) FMOC-DL-PIPECOLIC ACID FMOC-L-PIPECOLIC ACID 4-ALKOXYBENZYL ALCOHOL RESIN,FMOC-L-PIPECOLIC ACID-WANG RESIN FMOC-(2S)-(CIS/TRANS)-HOMOPRO(4-CH2CO2H) FMOC-L-TRANSHOMOPRO(4-N-AMIDINO-PMC) FMOC-L-HOMOPRO(4,4-DIFLUORO) FMOC-L-TRANSHOMOPRO(4-NH-ALLOC) FMOC-(2S)-(4-CIS/TRANS)-HOMOPRO(4-CH2OH) FMOC-L-TRANSHOMOPRO(4-NHBOC) (2S4R)-N1-(9-FLUORENYLMETHYLOXYCARBONYL)-4-(T-BUTYLOXYCARBONYLAMINOMETHYL)-PIPERIDINE-2-CARBOXYLIC ACID FMOC-L-(4-CIS/TRANS)-HOMOPRO(4-CH2NH-BOC)

(D)-N-(9-FLUORENYLMETHYLOXYCARBONYL)PIPECOLIC ACID

(D)-N-FMOC-PIPECOLIC ACID

FMOC-(R)-PIPECOLINIC ACID

FMOC-(R)-(+)-PIPERIDINE-2-CARBOXYLIC ACID

FMOC-(R)-PIPERIDINE-2-CARBOXYLIC ACID

FMOC-D-PIP-OH

FMOC-D-PIC(2)-OH

FMOC-D-HOMOPRO-OH

FMOC-D-HOMOPROLINE

FMOC-D-HOPRO-OH

(2R)-1-[(9H-FLUOREN-9-YLMETHOXY)CARBONYL]PIPERIDINE-2-CARBOXYLIC ACID

(2R)-1-[(9H-FLUOREN-9-YLMETHOXY)CARBONYL]HEXAHYDROPYRIDINE-2-CARBOXYLIC ACID

D-1-CBZ-PIPECOLINIC ACID

N-FMoc-DL-pipecolic acid, 96+%

N-FMoc-piperidine-2-carboxylic acid

N-FMoc-2-piperidinecarboxylic acid

DL-Fmoc-pipecolic acid

1,2-Piperidinedicarboxylic acid, 1-(9H-fluoren-9-ylmethyl) ester

N-Fmoc-piperidine-2-carboxylic acid 97%

2-(((9H-fluoren-9-yl)methoxy)carbonyl)piperidine-2-carboxylic acid

N-Fmoc-DL-pipecolic acid

N-ALPHA-(9-FLUORENYLMETHOXYCARBONYL)-D-HOMOPROLINE

N-ALPHA-(9-FLUORENYLMETHOXYCARBONYL)-D-PIPECOLIC ACID

N-ALPHA-FMOC-D-PIPECOLIC ACID

N-FMOC-(R)-PIPECOLINIC ACID

N-FMOC-D-PIPECOLINIC ACID

RARECHEM AR PA 0006

(R)-N-(9-FLUORENYLMETHYLOXYCARBONYL)-PIPERIDINE-2-CARBOXYLIC ACID

(R)-N-FLUORENYLMETHOXYCARBONYL-2-PIPERIDINECARBOXYLIC ACID

(R)-PIPERIDINE-1,2-DICARBOXYLIC ACID 1-(9H-FLUOREN-9-YLMETHYL) ESTER

N-(9-Fluorenylmethoxycarbonyl)-DL-homoproline

1-(9H-Fluoren-9-ylmethyl) 1,2-piperidinedicarboxylate

105751-19-7

Specialty Synthesis

Proline Derivatives

Peptide Synthesis

Unnatural Amino Acid Derivatives