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(R)-N-Cbz-3,4-Dihydro-1H-isoquinolinecarboxylic acid is a chemical compound that belongs to the isoquinoline group, which are heterocyclic aromatic organic compounds. It features the (R)-configuration, indicating its specific spatial orientation, and contains a Carboxybenzyl (Cbz) protecting group that is commonly used in organic chemistry to shield amine functional groups. (R)-N-Cbz-3,4-Dihydro-1H-isoquinolinecarboxylic acid is predominantly utilized in scientific research for the synthesis of more complex compounds.

151004-88-5

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151004-88-5 Usage

Uses

Used in Scientific Research:
(R)-N-Cbz-3,4-Dihydro-1H-isoquinolinecarboxylic acid is used as an intermediate compound for the synthesis of more complex organic compounds, facilitating the development of new chemical entities and materials in the field of chemistry.
Used in Pharmaceutical Industry:
(R)-N-Cbz-3,4-Dihydro-1H-isoquinolinecarboxylic acid is used as a building block in the synthesis of pharmaceutical compounds, contributing to the creation of new drugs and therapeutic agents.
Used in Chemical Synthesis:
(R)-N-Cbz-3,4-Dihydro-1H-isoquinolinecarboxylic acid is used as a reagent in various chemical reactions, enabling the production of a wide range of chemical products with potential applications in different industries.

Check Digit Verification of cas no

The CAS Registry Mumber 151004-88-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,1,0,0 and 4 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 151004-88:
(8*1)+(7*5)+(6*1)+(5*0)+(4*0)+(3*4)+(2*8)+(1*8)=85
85 % 10 = 5
So 151004-88-5 is a valid CAS Registry Number.
InChI:InChI=1/C18H17NO4/c20-17(21)16-15-9-5-4-8-14(15)10-11-19(16)18(22)23-12-13-6-2-1-3-7-13/h1-9,16H,10-12H2,(H,20,21)/t16-/m1/s1

151004-88-5SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name (R)-N-Cbz-3,4-dihydro-1H-isoquinolinecarboxylic acid

1.2 Other means of identification

Product number -
Other names (1R)-2-phenylmethoxycarbonyl-3,4-dihydro-1H-isoquinoline-1-carboxylic acid

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:151004-88-5 SDS

151004-88-5Relevant academic research and scientific papers

Enantioselective addition of vinylzinc reagents to 3,4-dihydroisoquinoline N-oxide

Wang, Sa,Seto, Christopher T.

, p. 3979 - 3982 (2007/10/03)

Ligand 2a promotes the enantioselective addition of vinylzinc reagents to 3,4-dihydroisoquinoline N-oxide to yield chiral allylic hydroxylamines. With 0.1 equiv of the ligand, the product is obtained in up to 84% ee, whereas with 1.2 equiv of the ligand,

PYRIMIDINE-2,4-DIONE DERIVATIVES AS GONADOTROPIN-RELEASING HORMONE RECEPTOR ANTAGONISTS

-

Page 55, (2008/06/13)

GnRH receptor antagonists are disclosed that have utility in the treatment of a variety of sex-hormone related conditions in both men and women. The compounds of this invention have the structure formula (I) wherein R1a, R1b, R2a, R2b, R3, R4, R5, R6, R7 and X are as defined herein, including stereoisomers, prodrugs and pharmaceutically acceptable salts thereof. Also disclosed are compositions containing a compound of this invention in combination with a pharmaceutically acceptable carrier, as well as methods relating to the use thereof for antagonizing gonadotropin-releasing hormone in a subject in need thereof.

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