214930
1,2,3,4-Tetrahydro-3-isoquinolinecarboxylic acid hydrochloride
96%
๋ก๊ทธ์ธ์กฐ์ง ๋ฐ ๊ณ์ฝ ๊ฐ๊ฒฉ ๋ณด๊ธฐ
๋ชจ๋ ์ฌ์ง(1)
About This Item
์คํ์(Hill ํ๊ธฐ๋ฒ):
C10H11NO2 ยท HCl
CAS Number:
Molecular Weight:
213.66
Beilstein:
3723332
EC Number:
MDL number:
UNSPSC ์ฝ๋:
12352100
PubChem Substance ID:
NACRES:
NA.22
์ถ์ฒ ์ ํ
![1,3-Bis[4-(dimethylamino)phenyl]-2,4-dihydroxycyclobutenediylium dihydroxide, bis(inner salt) Dye content 90 %](/deepweb/assets/sigmaaldrich/product/structures/301/519/500149b3-198c-44cf-b952-7e91f54fc48e/640/500149b3-198c-44cf-b952-7e91f54fc48e.png)
![2,4-Bis[4-(N,N-diphenylamino)-2,6-dihydroxyphenyl]squaraine 98%](/deepweb/assets/sigmaaldrich/product/structures/303/054/d8b9c845-3623-4f5a-8a30-ab6731034171/640/d8b9c845-3623-4f5a-8a30-ab6731034171.png)
๋ถ์
96%
mp
>300 ยฐC (lit.)
SMILES string
Cl[H].OC(=O)C1Cc2ccccc2CN1
InChI
1S/C10H11NO2.ClH/c12-10(13)9-5-7-3-1-2-4-8(7)6-11-9;/h1-4,9,11H,5-6H2,(H,12,13);1H
InChI key
FXHCFPUEIDRTMR-UHFFFAOYSA-N
์ ์ฌํ ์ ํ์ ์ฐพ์ผ์ญ๋๊น? ๋ฐฉ๋ฌธ ์ ํ ๋น๊ต ์๋ด
์ ํ๋ฆฌ์ผ์ด์
1,2,3,4-Tetrahydro-3-isoquinolinecarboxylic acid was used in the synthesis of 10,10a-dihydroimidazo-[1,5-b]isoquinoline-1,3(2H,5H)-diones, inhibitor of inflammation, apoprotein B-100 biosynthesis and matrix-degrading metalloprotienase.
์ ํธ์ด
Warning
์ ํด ๋ฐ ์ํ ์ฑ๋ช ์
์๋ฐฉ์กฐ์น ์ฑ๋ช ์
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
ํ์ ๊ธฐ๊ด
Respiratory system
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Flash Point (ยฐF)
Not applicable
Flash Point (ยฐC)
Not applicable
๊ฐ์ธ ๋ณดํธ ์ฅ๋น
dust mask type N95 (US), Eyeshields, Gloves
๊ฐ์ฅ ์ต์ ๋ฒ์ ์ค ํ๋๋ฅผ ์ ํํ์ธ์:
์ด ์ ํ์ ์ด๋ฏธ ๊ฐ์ง๊ณ ๊ณ์ญ๋๊น?
๋ฌธ์ ๋ผ์ด๋ธ๋ฌ๋ฆฌ์์ ์ต๊ทผ์ ๊ตฌ๋งคํ ์ ํ์ ๋ํ ๋ฌธ์๋ฅผ ์ฐพ์๋ณด์ธ์.
Alan R Katritzky et al.
The Journal of organic chemistry, 67(23), 8224-8229 (2002-11-09)
Condensations of chiral diamines 11a-c with benzotriazole and formaldehyde gave benzotriazolyl intermediates 12a-c; similar condensations of alpha-amino-amides 10a-c with benzotriazole and paraformaldehyde gave 14a-c. Subsequent treatment of 12a-c and 14a-c with AlCl(3) led to enantiopure tricyclic 1,2,3,5,10,10a-hexahydroimidazo[1,5-b]isoquinolines 1a-c and 2,3,10,10a-tetrahydroimidazo[1,5-b]isoquinolin-1(5H)-ones
Raman K Bakshi et al.
Bioorganic & medicinal chemistry letters, 15(14), 3430-3433 (2005-06-14)
The discovery of 1-amino-1,2,3,4-tetrahydronaphthalene-2-carboxylic acid analogs as potent human melanocortin-4 selective agonists is described.
B C Wilkes et al.
Biopolymers, 34(9), 1213-1219 (1994-09-01)
A molecular mechanics study (grid search and energy minimization) of the highly delta receptor-selective delta opioid antagonist H-Tyr-Tic-Phe-OH (TIP; Tic: tetrahydroisoquinoline-3-carboxylic acid) resulted in four low energy conformers with energies within 2 kcal/mol of that of the lowest energy structure.
M Manning et al.
Journal of peptide science : an official publication of the European Peptide Society, 1(1), 66-79 (1995-01-01)
We have investigated the effects of mono-substitutions with the conformationally restricted amino acid, 1,2,3,4 tetrahydroisoquinoline-3-carboxylic acid (Tic) at position 3 in arginine vasopressin (AVP), at positions 2, 3 and 7 in potent non-selective cyclic AVP V2/V1a antagonists, in potent and
Yingjie Zhang et al.
Current protein & peptide science, 11(8), 752-758 (2011-01-18)
Tic, short for 1,2,3,4-tetrahydroisoquinoline-3-carboxylic acid, is a kind of unnatural ฮฑ-amino acids. Due to its distinct geometrical conformation and biological activity, the structure of Tic, regarded as the surrogate of proline and the rigid analogue of phenylalanine or tyrosine, has
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