BOC-TIC-OH

ChemicalBook > CAS DataBase List > BOC-TIC-OH

Product Name: BOC-TIC-OH
CAS No.: 78879-20-6
Chemical Name: BOC-TIC-OH
Synonyms: Boc-Tic;BOC-L-TIC;BOC-TIC-OH;BOC-L-TIC-OH;Boc-Tic-OH, >=98%;RARECHEM BK PT 0083;BOC-TIC-OH USP/EP/BP;Boc-Tic-OH >=97.0% (TLC);(Tert-Butoxy)Carbonyl Tic-OH;Boc-L-Tetrahydroisoquinoline-3-COOH
CBNumber: CB4750051
Molecular Formula: C15H19NO4
Formula Weight: 277.32
MOL File: 78879-20-6.mol

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BOC-TIC-OH Property

Melting point:: 125-126.5 °C
Boiling point:: 420.18°C (rough estimate)
Density: 1.1311 (rough estimate)
refractive index: 1.5080 (estimate)
storage temp.: Sealed in dry,2-8°C
solubility: soluble in Methanol
pka: 3.88±0.20(Predicted)
form: Solid
color: White to off-white
optical activity: [α]20/D +19.0±1.5°, c = 0.7% in methanol
BRN: 4297114

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Safety

Hazard Codes: Xi
Safety Statements: 22-24/25
WGK Germany: 3
HazardClass: IRRITANT
HS Code: 29334900

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Hazard and Precautionary Statements (GHS)

Symbol(GHS)

Signal word

Warning

Hazard statements

H315Causes skin irritation

H319Causes serious eye irritation

Precautionary statements

P264Wash hands thoroughly after handling.

P264Wash skin thouroughly after handling.

P280Wear protective gloves/protective clothing/eye protection/face protection.

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N-Bromosuccinimide Price

TCI Chemical

Product number: B4501
Product name: (S)-2-(tert-Butoxycarbonyl)-1,2,3,4-tetrahydroisoquinoline-3-carboxylic Acid
Purity: >98.0%(HPLC)(T)
Packaging: 5g
Price: $94
Updated: 2024/03/01

TCI Chemical

Product number: B4501
Product name: (S)-2-(tert-Butoxycarbonyl)-1,2,3,4-tetrahydroisoquinoline-3-carboxylic Acid
Purity: >98.0%(HPLC)(T)
Packaging: 25g
Price: $277
Updated: 2024/03/01

Alfa Aesar

Product number: H61423
Product name: (S)-N-Boc-1,2,3,4-tetrahydroisoquinoline-3-carboxylic acid, 98%
Packaging: 1g
Price: $26.25
Updated: 2023/01/06

Alfa Aesar

Product number: H61423
Product name: (S)-N-Boc-1,2,3,4-tetrahydroisoquinoline-3-carboxylic acid, 98%
Packaging: 5g
Price: $81.06
Updated: 2023/01/06

Alfa Aesar

Product number: H61423
Product name: (S)-N-Boc-1,2,3,4-tetrahydroisoquinoline-3-carboxylic acid, 98%
Packaging: 25g
Price: $314
Updated: 2022/04/27

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BOC-TIC-OH Chemical Properties,Usage,Production

Chemical Properties

white to light beige powder

Uses

Boc-Tic-OH, is an amino acid building block used in peptide synthesis. With a growing peptide drug market the fast, reliable synthesis of peptides is of great importance.

BOC-TIC-OH Preparation Products And Raw materials

Raw materials

Preparation Products

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BOC-TIC-OH Suppliers

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View Lastest Price from BOC-TIC-OH manufacturers

Sichuan HongRi Pharma-Tech Co.,Ltd

Product: Boc-Tic-OH 78879-20-6
Price: US $0.00-0.00/kg
Min. Order: 1kg
Purity: 98%
Supply Ability: 1T
Release date: 2023-11-16

Career Henan Chemical Co

Product: BOC-TIC-OH 78879-20-6
Price: US $1.00/kg
Min. Order: 1kg
Purity: 98%
Supply Ability: 100KG
Release date: 2018-12-22

78879-20-6, BOC-TIC-OHRelated Search:

BOC-L-TYROSINE ETHYL ESTER Boc-L-serine methyl ester Boc-L-Tyrosine methyl ester BOC-VAL-NH2 BOC-SER-OH N-Boc-L-tert-Leucine N-Boc-L-valine BOC-L-TYR-OL BOC-TRP-OME Boc-L-Threonine BOC-L-Tyrosine O-(2-Azido-4,6-O-benzylidene-2-deoxy-alpha-D-galactopyranosyl)-N-Fmoc-L-serine tert-Butyl Ester 5,6,7,8-TETRAHYDROISOQUINOLINE L-1,2,3,4-Tetrahydroisoquinoline-3-carboxylic acid 1,2,3,4-TETRAHYDROISOQUINOLINE H-TIC-OH

Boc-(3S)-1,2,3,4-Tetrahydroisoquinoline-3-carboxylic acid98+%

(S)-N-Boc-1,2,3,4-tetrahydroisoquinoline-3-carboxylic A cid,99%e.e.

(Tert-Butoxy)Carbonyl Tic-OH

Boc-Tic

N-Boc-(S)-1,2,3,4-tetrahydroisoquinoline-3-carboxylic acid, 98%

N-T-BUTOXYCARBONYL-1,2,3,4-TETRAHYDROISOQUINOLINE-3-CARBOXYLIC ACID

(S)-()-N-BOC-1,2,3,4-TETRAHYDRO-3-ISOQUINOLINECARBOXYLIC ACID

(S)-(+)-N-BOC-1,2,3,4-TETRAHYDRO-3-ISOQUINOLINECARBOXYLIC ACID

(S)-N-BOC-1,2,3,4-TETRAHYDROISOQUINOLINE-3-CARBOXYLIC ACID

RARECHEM BK PT 0083

(S)-2-BOC-1,2,3,4-TETRAHYDROISOQUINOLINE-3-CARBOXYLIC ACID

(S)-(+)-2-(TERT-BUTOXYCARBONYL)-1,2,3,4-TETRAHYDRO-3-ISOQUINOLINECARBOXYLIC ACID

(S)-3,4-DIHYDRO-1H-ISOQUINOLINE-2,3-DICARBOXYLIC ACID 2-TERT-BUTYL ESTER

BOC-1,2,3,4-L-TETRAHYDROISOQUINOLINE-3-CARBOXYLIC ACID

BOC-(3S)-1,2,3,4-TETRAHYDROISOQUINOLINE-3-CARBOXYLIC ACID

Boc-Tic-OH >=97.0% (TLC)

Boc-Tic-OH, >=98%

(3S)-2-[(2-methylpropan-2-yl)oxy-oxomethyl]-3,4-dihydro-1H-isoquinoline-3-carboxylate

N-tert-Butoxycarbonyl-L-1,2,3,4-tetrahydroisoquinoline-3-carboxylic acid

BOC-L-TETRAHYDROISOQUINOLINE-3-CARBOXYLIC ACID

BOC-L-TIC

BOC-L-TIC-OH

BOC-L-1,2,3,4-TETRAHYDROISOQUINOLINE-3-CARBOXYLIC ACID

BOC-TIC-OH

BOC-(S)-1,2,3,4-TETRAHYDROISOQUINOLINE-3-CARBOXYLIC ACID

2,3(1H)-ISOQUINOLINEDICARBOXYLIC ACID, 3,4-DIHYDRO-,2-(1,1-DIMETHYLETHYL) ESTER, (3S)-

(3S)-2-(TERT-BUTOXYCARBONYL)-1,2,3,4-TETRAHYDROISOQUINOLINE-3-CARBOXYLIC ACID

(S)-(+)-2-(Tertutoxycarbonyl)-1,2,3,4-tetrahydro-3-isoquinolinecarboxylic acid

(S)-1,2,3,4-Tetrahydroisoquinoline-3-carboxylic acid, N-BOC protected

(S)-2-(tert-butoxycarbonyl)-1,2,3,4-tetrahydroisoquinoline-3-carboxylic acid

N-T-BUTYLOXYCARBONYL-L-1,2,3,4-TETRAHYDROISOQUINOLINE-3-CARBOXYLIC ACID

BOC-1,2,3,4-TETRAHYDROISOQUINOLINE-3-CARBOXYLIC ACID

N-BOC-L-1,2,3,4-Tetrahydroisoquinoline-3-carboxylic acid,99%

Boc-(S)-1,2,3,4-tetrahydroisoquinoline-line-3-carboxylic acid

N-1-BOC-L-1,2,3,4-TETRAHYDRO-ISOQUINOLINE-3-CARBOXYLIC ACID

N-1-T-BOC-L-1,2,3,4-TETRAHYDRO-ISOQUINOLINE-3-CARBOXYLIC ACID

N-ALPHA-T-BOC-L-1,2,3,4-TETRAHYDRO-ISOQUINOLINE-3-CARBOXYLIC ACID

N-BOC-L-1,2,3,4-TETRAHYDROISOQUINOLINE-3-CARBOXYLIC ACID

N-TERT-BUTYLOXYCARBONYL-L-1,2,3,4-TETRAHYDROISOQUINOLINE-3-CARBOXYLIC ACID

N-Boc-L-1,2,3,4-Tetrahydroisoquinoline-3-carboxyli

N-T-boc-L-1,2,3,4-tetrahydroiso-*quinoline-3-carb

Boc-L-1,2,3,4-tetrahydroisoquinoline-3-carboxylic

(3S)-1,2,3,4-Tetrahydroisoquinoline-3-carboxylic acid, N-BOC protected

Boc-L-Tetrahydroisoquinoline-3-COOH

Boc-Tic-OH(Boc-1,2,3,4-Tetrahydroisoquinoline-3-carboxylic acid)

N-Boc-L-1,2,3,4-Tetrahydroisoquinoline-3-carboxyli acid

Boc-(S)-1,2,3,4-tetrahydroisoquinoline-3-carboxylicaci

BOC-TIC-OH USP/EP/BP

78879-20-6

78879-20-9

78879-20-8

78879-20-7

C15H19NO4

Peptide Synthesis

Others

Unnatural Amino Acid Derivatives

Specialty Synthesis

a-amino