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1305320-64-2

N-Boc-3-bromo-4-methylindole is a specialized chemical compound often utilized in the field of organic chemistry. The element indole in its structure exhibits bioactivity, which makes it critical in pharmaceutical applications. Its highly specific structure, characterized by a bromo and a methyl group in specific positions, requires sophisticated methods for its production. This chemical is generally protected by Boc (tert-butoxycarbonyl) group to prevent unwanted reactions. It is a chemical that requires careful handling due to its reactive nature and potential hazards associated with it. The comprehensive physicochemical, toxicological, and ecological characteristics of this chemical are not widely studied, thus warranting caution during its application.

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  • 1305320-64-2 Structure

  • Basic information

    1. Product Name: N-Boc-3-bromo-4-methylindole
    2. Synonyms: N-Boc-3-bromo-4-methylindole;tert-butyl 3-bromo-4-methyl-1H-indole-1-carboxylate
    3. CAS NO:1305320-64-2
    4. Molecular Formula: C14H16BrNO2
    5. Molecular Weight: 310.18634
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1305320-64-2.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 384.6±34.0 °C(Predicted)
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: 1.34±0.1 g/cm3(Predicted)
    6. Refractive Index: N/A
    7. Storage Temp.: 2-8°C
    8. Solubility: N/A
    9. CAS DataBase Reference: N-Boc-3-bromo-4-methylindole(CAS DataBase Reference)
    10. NIST Chemistry Reference: N-Boc-3-bromo-4-methylindole(1305320-64-2)
    11. EPA Substance Registry System: N-Boc-3-bromo-4-methylindole(1305320-64-2)

  • 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: 1305320-64-2(Hazardous Substances Data)

1305320-64-2 Usage

Uses

Used in Pharmaceutical Industry:
N-Boc-3-bromo-4-methylindole is used as an intermediate compound for the synthesis of various pharmaceuticals. Its bioactive indole structure and specific bromo and methyl groups make it a valuable building block in the development of new drugs.
Used in Organic Chemistry Research:
N-Boc-3-bromo-4-methylindole is used as a research compound in organic chemistry. Its unique structure and reactivity provide opportunities for studying complex chemical reactions and mechanisms, contributing to the advancement of the field.
Used in Chemical Synthesis:
N-Boc-3-bromo-4-methylindole is used as a key component in the synthesis of complex organic molecules. Its protected Boc group allows for selective reactions, making it a versatile building block in the creation of a wide range of chemical products.

Check Digit Verification of cas no

The CAS Registry Mumber 1305320-64-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,0,5,3,2 and 0 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1305320-64:
(9*1)+(8*3)+(7*0)+(6*5)+(5*3)+(4*2)+(3*0)+(2*6)+(1*4)=102
102 % 10 = 2
So 1305320-64-2 is a valid CAS Registry Number.

1305320-64-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-Methyl-2-propanyl 3-bromo-4-methyl-1H-indole-1-carboxylate

1.2 Other means of identification

Product number -
Other names -

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:1305320-64-2 SDS

1305320-64-2Downstream Products

1305320-64-2Relevant articles and documents

CYCLOHEXAPEPTIDES AS SELECTIVE SOMATOSTATIN SST5 RECEPTOR AGONISTS

-

, (2020/05/19)

The disclosures herein relate to novel compounds of formula (1) : (1) and salts thereof, wherein W, X, Y, Z, m, n, q, R1, R2, R3, R4, R5 and R6 are defined herein, and their use in treating

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