H-Tic-OH

Modify Date: 2024-01-05 12:17:51

H-Tic-OH Structure
H-Tic-OH structure
 Common Name H-Tic-OH
CAS Number 74163-81-8 Molecular Weight 177.20
Density 1.2±0.1 g/cm3 Boiling Point 372.0±42.0 °C at 760 mmHg
Molecular Formula C10H11NO2 Melting Point 300ºC
MSDS Chinese USA Flash Point 178.8±27.9 °C
Symbol GHS07
GHS07		 Signal Word Warning

 Use of H-Tic-OH


L-Porretine is a biochemical reagent that can be used as a biological material or organic compound for life science related research.

 Names

Name (S)-(-)-1,2,3,4-Tetrahydroisoquinoline-3-Carboxylic Acid
Synonym More Synonyms

 H-Tic-OH Biological Activity

Description L-Porretine is a biochemical reagent that can be used as a biological material or organic compound for life science related research.
Related Catalog
In Vitro 一种抗酶促降解的受限苯丙氨酸类似物。

 Chemical & Physical Properties

Density 1.2±0.1 g/cm3
Boiling Point 372.0±42.0 °C at 760 mmHg
Melting Point 300ºC
Molecular Formula C10H11NO2
Molecular Weight 177.20
Flash Point 178.8±27.9 °C
Exact Mass 177.078979
PSA 49.33000
LogP 0.86
Vapour Pressure 0.0±0.9 mmHg at 25°C
Index of Refraction 1.577
Storage condition 2~8°C

 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 Xi:Irritant
Risk Phrases R36/37/38
Safety Phrases S26-S37/39
RIDADR NONH for all modes of transport
WGK Germany 3
HS Code 2933499090

 Synthetic Route

 Customs

HS Code 2933499090
Summary 2933499090. other compounds containing in the structure a quinoline or isoquinoline ring-system (whether or not hydrogenated), not further fused. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:20.0%

 Articles21

More Articles
Acid catalysis in the formation of dioxopiperazines from peptides containing tetrahydroisoquinoline-3-carboxylic acid at position 2.

Int. J. Pept. Protein Res. 45(6) , 567-73, (1995)

The kinetics of the spontaneous formation of 2,5-dioxopiperazines from peptides containing the Tic (1,2,3,4-tetrahydroisoquinoline-3-carboxylic acid) residue in the 2-position of the sequence has been...

2-Substituted (S)-2-(3,3-dimethyl-1-oxo-10,10a-dihydroimidazo[1,5-b]isoquinolin-2(1H,3H,5H)-yl)acetic acids: Conformational prediction, synthesis, anti-thrombotic and vasodilative evaluation.

Bioorg. Med. Chem. 19 , 871-82, (2011)

(S)-1,2,3,4-Tetrahydroisoquinoline-3-carboxylic acid (TIC) can inhibit thrombosis by inhibiting platelet aggregation. The investigation of amino acids modified TIC reveals that a stretching conformati...

Constrained phenylalanine analogues. Preferred conformation of the 1,2,3,4-tetrahydroisoquinoline-3-carboxylic acid (Tic) residue.

Int. J. Pept. Protein Res. 40 , 222, (1992)

Three Tic-containing (Tic = 1,2,3,4-tetrahydroisoquinoline-3-carboxylic acid) model peptides were synthesized to assess the tendency of this constrained Phe analogue to fold into a beta-bend and a hel...

 Synonyms

(3S)-1,2,3,4-Tetrahydro-3-isoquinolinecarboxylic acid
3-Isoquinolinecarboxylic acid, 1,2,3,4-tetrahydro-, (3S)-
(3S)-1,2,3,4-Tetrahydroisoquinoline-3-carboxylic acid
MFCD00800357
H-Tic-OH
L-1,2,3,4-Tetrahydroisoquinoline-3-carboxylic acid
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Chemsrc provides H-Tic-OH(CAS#:74163-81-8) MSDS, density, melting point, boiling point, structure, formula, molecular weight etc. Articles of H-Tic-OH are included as well.>> amp version: H-Tic-OH

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