(S)-1-Boc-piperidine-2-carboxylic acid

Modify Date: 2024-01-02 07:25:02

(S)-1-Boc-piperidine-2-carboxylic acid Structure
(S)-1-Boc-piperidine-2-carboxylic acid structure
Common Name (S)-1-Boc-piperidine-2-carboxylic acid
CAS Number 26250-84-0 Molecular Weight 229.27
Density 1.2±0.1 g/cm3 Boiling Point 353.2±35.0 °C at 760 mmHg
Molecular Formula C11H19NO4 Melting Point 122-126 °C(lit.)
MSDS Chinese USA Flash Point 167.4±25.9 °C
Symbol GHS07
GHS07
Signal Word Warning

 Use of (S)-1-Boc-piperidine-2-carboxylic acid


Boc-Pip-OH (Boc-L-pipecolic acid) is a biochemical reagent that can be used as a biological material or organic compound for life science related research.

 Names

Name (2S)-1-[(2-methylpropan-2-yl)oxycarbonyl]piperidine-2-carboxylic acid
Synonym More Synonyms

 (S)-1-Boc-piperidine-2-carboxylic acid Biological Activity

Description Boc-Pip-OH (Boc-L-pipecolic acid) is a biochemical reagent that can be used as a biological material or organic compound for life science related research.
Related Catalog

 Chemical & Physical Properties

Density 1.2±0.1 g/cm3
Boiling Point 353.2±35.0 °C at 760 mmHg
Melting Point 122-126 °C(lit.)
Molecular Formula C11H19NO4
Molecular Weight 229.27
Flash Point 167.4±25.9 °C
Exact Mass 229.131409
PSA 66.84000
LogP 1.13
Vapour Pressure 0.0±1.7 mmHg at 25°C
Index of Refraction 1.496

 Safety Information

Symbol GHS07
GHS07
Signal Word Warning
Hazard Statements H315-H319-H335
Precautionary Statements P261-P305 + P351 + P338
Personal Protective Equipment dust mask type N95 (US);Eyeshields;Gloves
Hazard Codes Xn:Harmful;
Risk Phrases R22;R36/37/38
Safety Phrases S26-S36-S36/37/39-S22
RIDADR NONH for all modes of transport
WGK Germany 3
HS Code 2933399090

 Synthetic Route

 Customs

HS Code 2933399090
Summary 2933399090. other compounds containing an unfused pyridine ring (whether or not hydrogenated) in the structure. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:20.0%

 Synonyms

(S)-(-)-1-(tert-butoxycarbonyl)-2-piperidine carboxylic acid
1,2-Piperidinedicarboxylic acid, 1-(1,1-dimethylethyl) ester
1-{[(2-Methyl-2-propanyl)oxy]carbonyl}-2-piperidinecarboxylic acid
(S)-piperidine-1,2-dicarboxylic acid 1-tert-butyl ester
(S)-1-(tert-butyloxycarbonyl)piperidine-2-carboxylic acid
S-N-Boc-Piperidine-2-carboxylic acid
(2S)-1-(tert-Butoxycarbonyl)-2-piperidinecarboxylic acid
(S)-1-N-Boc-piperidine-2-carboxylic acid
(S)-1-(tert-Butoxycarbonyl)piperidine-2-carboxylic acid
(S)-N-Boc-2-piperidinecarboxylic acid
(S)-N-Boc-piperidine-2-carboxylic acid
Boc-L-Pipecolic acid
BOC-L-Homoproline
boc-l-piperidine-2-carboxylic acid
(S)-1-Boc-2-piperidinecarboxylic acid
(S)-1-(tert-Butoxycarbonyl)-2-piperidinecarboxylic Acid
Boc-Pip-OH
1-Boc-L-pipecolic Acid
Boc-Beta-Homo-Pro-OH
(L)-N-Boc-Pipecolic acid
MFCD00151904
1-tert-Butyloxycarbonyl-L-pipecolinic acid
2S-N-(t-Butoxycarbonyl)-piperidine-2-carboxylic acid
boc-l-pip-oh
1-(tert-Butoxycarbonyl)-L-pipecolic Acid
1,2-Piperidinedicarboxylic acid, 1-(1,1-dimethylethyl) ester, (2S)-
1-(tert-Butoxycarbonyl)piperidine-2-carboxylic acid
N-Boc-L-pipecolinic acid
(S)-1-Boc-piperidine-2-carboxylic acid
Boc-β-Homo-Pro-OH
Boc-HomoPro-OH
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