What is the H-TRP(BOC)-OH?

H-TRP(BOC)-OH is , while it's Molecular Formula is C 16 H 20 N 2 O 4 .

What is the CAS number for H-TRP(BOC)-OH?

The CAS number of H-TRP(BOC)-OH is 146645-63-8.

What is the H-TRP(BOC)-OH?

H-TRP(BOC)-OH is , while it's Molecular Formula is C 16 H 20 N 2 O 4 .

What is the CAS number for H-TRP(BOC)-OH?

The CAS number of H-TRP(BOC)-OH is 146645-63-8.

High Purity N-Indole-T-Boc-L-tryptophan 146645-63-8 Factory Price

Product Details

Quick Details

CasNo： 146645-63-8
Molecular Formula： C16H20N2O4
Purity： 99%

High Purity N-Indole-T-Boc-L-tryptophan 146645-63-8 Factory Price

Molecular Formula:C₁₆H₂₀N₂O₄
Molecular Weight:304.346
Vapor Pressure:0mmHg at 25°C
Boiling Point:476.718°C at 760 mmHg
PKA:2.21±0.10(Predicted)
Flash Point:242.11°C
PSA：94.55000
Density:1.258g/cm³
LogP:3.07920

H-TRP(BOC)-OH(Cas 146645-63-8) Usage

Chemical Properties

White to off white powder

InChI:InChI=1/C16H20N2O4/c1-16(2,3)22-15(21)18-9-10(8-12(17)14(19)20)11-6-4-5-7-13(11)18/h4-7,9,12H,8,17H2,1-3H3,(H,19,20)/t12-/m0/s1

146645-63-8 Relevant articles

Method for preparing pharmaceutical intermediate of tryptophan derivative

-

Paragraph 0086; 0088; 0111-0114, (2021/09/21)

The synthesis method comprises the follo...

Thermal cleavage of the Fmoc protection group

Hoeck, Stefan,Marti, Roger,Riedl, Rainer,Simeunovic, Marina

experimental part, p. 200 - 202 (2011/08/05)

The Fmoc protection group is among the m...

146645-63-8 Process route

: 143824-78-6,163619-04-3
3-[(S)-2-carboxy-2-(9H-fluoren-9-ylmethoxycarbonylamino)ethyl]indole-1-carboxylic acid tert-butyl ester

: 4425-82-5
9-methylene-fluorene

: 146645-63-8
(2S)-2-amino-3-(1-tert-butoxycarbonylindol-3-yl)propanoic acid

: 73-22-3,27732-43-0,80206-30-0,27813-82-7
L-Tryptophan

Conditions

Conditions	Yield
With dimethyl sulfoxide; at 120 ℃; for 0.333333h; Microwave irradiation;

: 96238-70-9
1-tert-butoxycarbonyl-L-tryptophane methyl ester

: 146645-63-8
(2S)-2-amino-3-(1-tert-butoxycarbonylindol-3-yl)propanoic acid

Conditions

Conditions	Yield
With water; potassium carbonate; In methanol; at 20 ℃;	93%

146645-63-8 Upstream products

143824-78-6
3-[(S)-2-carboxy-2-(9H-fluoren-9-ylmethoxycarbonylamino)ethyl]indole-1-carboxylic acid tert-butyl ester
1604-49-5
methyl (2S)-3-(1H-indol-3-yl)-2-(trifluoroacetamido)propanoate
2717-76-2
(S)-N-benzyloxycarbonyl-L-tryptophan methyl ester
643751-42-2
N-carbobenzyloxy-1-tert-butoxycarbonyl-L-tryptophan methyl ester

146645-63-8 Downstream products

197632-75-0
1-[(1,1-dimethylethoxy)carbonyl]-N-[(9H-fluoren-9-ylmethoxy)carbonyl]-N-methyl-L-tryptophan
143824-78-6
3-[(S)-2-carboxy-2-(9H-fluoren-9-ylmethoxycarbonylamino)ethyl]indole-1-carboxylic acid tert-butyl ester
16765-79-0
1-phenyl-9H-pyrido[3,4-b]indole
552332-77-1
(2S)-2-amino-4-phenyl-N-{5-[(E)-2-pyridin-4-ylvinyl]pyridin-3-yl}butanamide

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146645-63-8

Quick Details

High Purity N-Indole-T-Boc-L-tryptophan 146645-63-8 Factory Price

H-TRP(BOC)-OH(Cas 146645-63-8) Usage

146645-63-8 Relevant articles

Method for preparing pharmaceutical intermediate of tryptophan derivative

-

Paragraph 0086; 0088; 0111-0114, (2021/09/21)

Thermal cleavage of the Fmoc protection group

Hoeck, Stefan,Marti, Roger,Riedl, Rainer,Simeunovic, Marina

experimental part, p. 200 - 202 (2011/08/05)

146645-63-8 Process route

146645-63-8 Upstream products

146645-63-8 Downstream products

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