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Tert-butyl 5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-3,4-dihydroisoquinoline-2(1H)-carboxylate is a white solid organic compound that is a member of the phenolic glycosides class. It exhibits limited solubility in water but is soluble in organic solvents like ethanol. tert-butyl 5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-3,4-dihydroisoquinoline-2(1H)-carboxylate is characterized by its potential to serve as a ligand in catalytic systems and its strong binding affinity to various biological receptors, which makes it a valuable intermediate in the synthesis of pharmaceuticals and other biologically active compounds.

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  • tert-butyl 5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-3,4-dihydro-1H-isoquinoline-2-carboxylate

    Cas No: 1035235-26-7

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  • tert-butyl 5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-3,4-dihydroisoquinoline-2(1H)-carboxylate

    Cas No: 1035235-26-7

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  • tert-Butyl 5-(4,4,5,5-tetraMethyl-1,3,2-dioxaborolan-2-yl)-3,4-dihydroisoquinoline-2(1H)-carboxylate

    Cas No: 1035235-26-7

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  • 1035235-26-7 Structure
  • Basic information

    1. Product Name: tert-Butyl 5-(4,4,5,5-tetraMethyl-1,3,2-dioxaborolan-2-yl)-3,4-dihydroisoquinoline-2(1H)-carboxylate
    2. Synonyms: tert-Butyl 5-(4,4,5,5-tetraMethyl-1,3,2-dioxaborolan-2-yl)-3,4-dihydroisoquinoline-2(1H)-carboxylate;tert-Butyl 5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-3,4-dihydroisoquinoline-2(1H)-carboxyl;2(1H)-Isoquinolinecarboxylic acid, 3,4-dihydro-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-, 1,1-dimethylethyl ester;2(1H)-Isoquinolinecarboxylic acid, 3,4-dihydro-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-, 1,1;tert-Butyl 5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-3,4-dihydroisoquinoline-2(1H)-carbo
    3. CAS NO:1035235-26-7
    4. Molecular Formula: C20H30BNO4
    5. Molecular Weight: 359.2675
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1035235-26-7.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: under inert gas (nitrogen or Argon) at 2-8°C
    8. Solubility: N/A
    9. CAS DataBase Reference: tert-Butyl 5-(4,4,5,5-tetraMethyl-1,3,2-dioxaborolan-2-yl)-3,4-dihydroisoquinoline-2(1H)-carboxylate(CAS DataBase Reference)
    10. NIST Chemistry Reference: tert-Butyl 5-(4,4,5,5-tetraMethyl-1,3,2-dioxaborolan-2-yl)-3,4-dihydroisoquinoline-2(1H)-carboxylate(1035235-26-7)
    11. EPA Substance Registry System: tert-Butyl 5-(4,4,5,5-tetraMethyl-1,3,2-dioxaborolan-2-yl)-3,4-dihydroisoquinoline-2(1H)-carboxylate(1035235-26-7)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 1035235-26-7(Hazardous Substances Data)

1035235-26-7 Usage

Uses

Used in Pharmaceutical Synthesis:
Tert-butyl 5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-3,4-dihydroisoquinoline-2(1H)-carboxylate is used as a key intermediate in the synthesis of pharmaceuticals for its ability to facilitate the creation of biologically active compounds.
Used in Catalytic Systems:
In the field of catalysis, this compound is used as a ligand, playing a crucial role in enhancing the efficiency and selectivity of various chemical reactions.
Used in Materials Science:
Tert-butyl 5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-3,4-dihydroisoquinoline-2(1H)-carboxylate is used in the development of new organic materials, where its unique properties and functionalities contribute to the advancement of material science.
Used in Medical Applications:
Due to its strong binding affinity with biological receptors, this compound has potential applications in medicine, although specific uses are not detailed in the provided materials. Its role in medicine would likely involve targeting specific receptors for therapeutic effects.

Check Digit Verification of cas no

The CAS Registry Mumber 1035235-26-7 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,3,5,2,3 and 5 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1035235-26:
(9*1)+(8*0)+(7*3)+(6*5)+(5*2)+(4*3)+(3*5)+(2*2)+(1*6)=107
107 % 10 = 7
So 1035235-26-7 is a valid CAS Registry Number.

1035235-26-7Downstream Products

1035235-26-7Relevant articles and documents

TRICYCLIC ATROPISOMER COMPOUNDS

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Page/Page column 57, (2016/06/06)

Disclosed are compounds of Formula (I): or a salt thereof, wherein Q is: or; and X, R1a, R1b, R3, R4, and R5 are defined herein. Also disclosed are methods of using such compounds as inhibitors of Bru

HETEROCYCLE SUBSTITUTED AMINO-PYRIDINE COMPOUNDS AND METHODS OF USE THEREOF

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Paragraph 0589; 0591, (2016/04/20)

The present disclosure relates to heterocycle substituted amino-pyridine compounds. The present disclosure also relates to pharmaceutical compositions containing these compounds and methods of treating cancer by administering these compounds and pharmaceutical compositions to subjects in need thereof. The present disclosure also relates to the use of such compounds for research or other non-therapeutic purposes.

SULFAMIDE SODIUM CHANNEL INHIBITORS

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Page/Page column 39, (2013/09/26)

The present invention provides compounds of Formula I, or pharmaceutically acceptable salts thereof, that are inhibitors of voltage-gated sodium channels, in particular Nav 1.7. The compounds are useful for the treatment of diseases treatable by inhibition of sodium channels such as pain disorders. Also provided are pharmaceutical compositions containing compounds of the present invention.

S1P1 AGONISTS COMPRISING A BICYCLIC N-CONTAINING RING

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, (2010/12/31)

The present invention relates to novel compounds of formula (I) having S1P1 agonist activity, processes for their preparation, pharmaceutical compositions containing them and their use in the treatment of various disorders.

THIAZOLE OR THIADIZALOE DERIVATIVES FOR USE AS SPHINGOSINE 1-PHOSPHATE 1 (S1P1) RECEPTOR AGONISTS

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Page/Page column 38, (2010/12/31)

Thiazole or thiadizaloe derivatives of formula (I) or pharmaceutical salts thereof having pharmacological activity, processes for their preparation, pharmaceutical compositions containing them and their uses in the treatment of various disorders mediated

Certain pyrazoline derivatives with kinase inhibitory activity

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Page/Page column 102, (2008/12/06)

The present invention provides certain pyrazoline compounds useful as inhibitors of protein kinases. The invention also provides pharmaceutical compositions and methods of using the compositions in the treatment of various diseases.

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