66863-43-2(BOC-L-1,2,3,4-TETRAHYDRONORHARMAN-3-CARBOXYLIC ACID)
Product Description
66863-43-2
CAS No.
66863-43-2
Chemical Name:
BOC-L-1,2,3,4-TETRAHYDRONORHARMAN-3-CARBOXYLIC ACID
CBNumber:
CB0724991
Molecular Formula:
C17H20N2O4
Formula Weight:
316.35
MOL File:
Mol file
BOC-L-1,2,3,4-TETRAHYDRONORHARMAN-3-CARBOXYLIC ACID Synonyms:
RARECHEM BK PT 0089
(S)-2-BOC-1,2,3,4-TETRAHYDRONORHARMANE-3-CARBOXYLIC ACID
BOC-THNH(3)-OH
BOC-TPI-OH
BOC-L-TRYPTOLINE-3-CARBOXYLIC ACID
BOC-L-TPI
BOC-L-TPI-OH
BOC-L-1,2,3,4-TETRAHYDRO-9H-PYRIDO[3,4-B]INDOLE-3-CARBOXYLIC ACID
BOC-L-1,2,3,4-TETRAHYDRONORHARMAN-3-CARBOXYLIC ACID
Property
Melting point:
286-291 °C
Boiling point:
525.6±50.0 °C(Predicted)
Density
1.322±0.06 g/cm3(Predicted)
storage temp.
0-6°C
pka
3.98±0.20(Predicted)
BRN
691288
CAS DataBase Reference
66863-43-2(CAS DataBase Reference)
Safety
Hazard Codes :
Xi
Safety Statements :
24/25
HazardClass :
IRRITANT
HS Code :
29339900
BOC-L-1,2,3,4-TETRAHYDRONORHARMAN-3-CARBOXYLIC ACID
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Belgium 2
China 73
Europe 1
France 1
Germany 6
India 2
Japan 3
Switzerland 1
United Kingdom 2
United States 13
Global 104
Supplier
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Email
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Bide Pharmatech Ltd.
400-164-7117
product02@bidepharm.com
China
41463
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Hebei Zhentian Food Additives Co., Ltd.
0319-5925599
13933732699@163.com
China
12186
58
Hebei Zhentian food additives Co., LTD
0319-5925599
13933732699@163.com
China
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Shanghai Haohong Pharmaceutical Co., Ltd.
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China
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ZHEJIANG JIUZHOU CHEM CO., LTD
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Shanghai Sunway Pharmaceutical Technology Co., Ltd
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China
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Accela ChemBio Co.,Ltd.
021-50795510
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China
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Hubei wei shi reagent group ltd., company
027-59102966
2853877583@qq.com
China
2829
58
66863-43-2(BOC-L-1,2,3,4-TETRAHYDRONORHARMAN-3-CARBOXYLIC ACID)
Related Search:
RARECHEM BK PT 0089
(S)-2-BOC-1,2,3,4-TETRAHYDRONORHARMANE-3-CARBOXYLIC ACID
BOC-THNH(3)-OH
BOC-TPI-OH
BOC-L-TRYPTOLINE-3-CARBOXYLIC ACID
BOC-L-TPI
BOC-L-TPI-OH
BOC-L-1,2,3,4-TETRAHYDRO-9H-PYRIDO[3,4-B]INDOLE-3-CARBOXYLIC ACID
BOC-L-1,2,3,4-TETRAHYDRONORHARMAN-3-CARBOXYLIC ACID
N-ALPHA-(T-BUTYLOXYCARBONYL)-1,2,3,4-TETRAHYDRONORHARMAN-L-3-CARBOXYLIC ACID
N-ALPHA-TERT-BUTYLOXYCARBONYL-1,2,3,4-TETRAHYDRONORHARMAN-L-3-CARBOXYLIC ACID
N-ALPHA-T-BUTOXYCARBONYL-L-1,2,3,4-TETRAHYDRO-BETA-CARBOLINE-3-CARBOXYLIC ACID
N-ALPHA-T-BUTOXYCARBONYL-L-1,2,3,4-TETRAHYDRONORHARMAN-3-CARBOXYLIC ACID
N-ALPHA-T-BUTOXYCARBONYL-L-TRYPTOLINE-3-CARBOXYLIC ACID
N-BOC-L-1,2,3,4-TETRAHYDRO-9H-PYRIDO-[3,4-B]-INDOLE-3-CARBOXYLIC ACID
N-BOC-L-1,2,3,4-TETRAHYDRO-BETA-CARBOLINE-3-CARBOXYLIC ACID
N-α-Boc-L-1,2,3,4-tetrahydronorharmane-3-carboxylic acid
Boc-L-1,2,3,4-Tetrahydro-b-Carbolin-3-CarboxylicAcid
n-(tert-butoxycarbonyl)-l-1,2,3,4-tetrahydronorharman-3-carboxylic acid
n-boc-l-1,2,3,4-tetrahydronorharman-3-carboxylic acid
(S)-1,2,3,4-Tetrahydronorharman-3-carboxylic acid, N2-BOC protected
(S)-2-(tert-Butoxycarbonyl)-2,3,4,9-tetrahydro-1H-pyrido[3,4-b]indole-3-carboxylic acid
N-.ALPHA.-BOC-L-1,2,3,4-TETRAHYDRONORHARMANE-3-CARBOXYLIC ACID
Boc-L-1,2,3,4-tetrahydro-9H-pyrido[3,4-b]indole-3-
N-BOC-L-1,2,3,4-Tetrahydro-beta-carboline-3-carboxylic acid,98%
N-α-Boc-L-1,2,3,4-tetrahydronorharmane-3-carboxyl
Boc-L-tryptoline-3-carboxylic acid, Boc-Tpi-OH, Boc-L-1,2,3,4-tetrahydro-9H-pyrido[3,4-b]indole-3-carboxylic acid, Boc-L-1,2,3,4-Tetrahydro-b-carboline-3-carboxylic acid
Boc-L-1,2,3,4-tetrahydronorharman-3-carboxylic acid≥ 98% (HPLC)
Boc-L-Tπ-OH
(3S)-1-(tert-Butoxycarbonyl)-2,3,4,9-tetrahydro-1H-pyrido[3,4-b]indole-3-carboxylic acid
(Tert-Butoxy)Carbonyl L-1,2,3,4-Tetrahydronorharman-3-carboxylic acid
N-Boc-(S)-2,3,4,9-Tetrahydro-β-carboline-3-carboxylic acid
(3S)-2-[(tert-butoxy)carbonyl]-1H,2H,3H,4H,9H-pyrido[3,4-b]indole-3-carboxylic acid
2H-Pyrido[3,4-b]indole-2,3-dicarboxylic acid, 1,3,4,9-tetrahydro-, 2-(1,1-dimethylethyl) ester, (3S)-
Boc-L-1,2,3,4-Tetrahydro-β-carbolin-3-carboxylic acid
BOC-L-1,2,3,4-TETRAHYDRONORHARMAN-3-CARBOXYLIC ACID USP/EP/BP
Boc-L-Tpi-OH (Boc-L-1,2,3,4-tetrahydronorharman-3-carboxylic acid)
(3S)-2-tert-butoxycarbonyl-1,3,4,9-tetrahydropyrido[3,4-b]indole-3-carboxylic acid
(S)-2-Boc-2,3,4,9-tetrahydro-1H-pyrido[3,4-b]indole-3-carboxylic Acid
66863-43-2
Others
Peptide Synthesis
Unnatural Amino Acid Derivatives
Phenylalanine analogs and other aromatic alpha amino acids
Amino Acid Derivatives
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