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1H-Indazole,6-chloro-4-iodois a chemical compound belonging to the indazole class, which is characterized by a bicyclic structure with two nitrogen atoms in the five-membered ring. The "1H" notation indicates the presence of a hydrogen atom, while the "6-chloro-4-iodo" denomination suggests that a chlorine atom is attached at position 6 and an iodine atom at position 4 in the indazole ring structure. 1H-Indazole,6-chloro-4-iodois often used in pharmaceutical research and the synthesis of various organic compounds, with its properties varying depending on its specific formulation. It is involved in sophisticated chemical reactions that require experienced handling.

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  • 885519-56-2 Structure
  • Basic information

    1. Product Name: 1H-Indazole,6-chloro-4-iodo-
    2. Synonyms: 1H-Indazole,6-chloro-4-iodo-
    3. CAS NO:885519-56-2
    4. Molecular Formula: C7H4ClIN2
    5. Molecular Weight: 278.47753
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 885519-56-2.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 388.2±22.0 °C(Predicted)
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: 2.156
    6. Refractive Index: N/A
    7. Storage Temp.: 2-8°C(protect from light)
    8. Solubility: N/A
    9. PKA: 11.78±0.40(Predicted)
    10. CAS DataBase Reference: 1H-Indazole,6-chloro-4-iodo-(CAS DataBase Reference)
    11. NIST Chemistry Reference: 1H-Indazole,6-chloro-4-iodo-(885519-56-2)
    12. EPA Substance Registry System: 1H-Indazole,6-chloro-4-iodo-(885519-56-2)
  • 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: 885519-56-2(Hazardous Substances Data)

885519-56-2 Usage

Uses

Used in Pharmaceutical Research:
1H-Indazole,6-chloro-4-iodois used as a research compound for the development of new pharmaceuticals, due to its unique chemical structure and potential interactions with biological targets.
Used in Organic Synthesis:
1H-Indazole,6-chloro-4-iodois used as a synthetic intermediate for the preparation of various organic compounds, leveraging its reactive functional groups and structural features to facilitate the synthesis of complex molecules.

Check Digit Verification of cas no

The CAS Registry Mumber 885519-56-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,8,5,5,1 and 9 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 885519-56:
(8*8)+(7*8)+(6*5)+(5*5)+(4*1)+(3*9)+(2*5)+(1*6)=222
222 % 10 = 2
So 885519-56-2 is a valid CAS Registry Number.

885519-56-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 6-Chloro-4-iodo-1H-indazole

1.2 Other means of identification

Product number -
Other names RW3742

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:885519-56-2 SDS

885519-56-2Relevant articles and documents

Application of C-H Functionalization in the Development of a Concise and Convergent Route to the Phosphatidylinositol-3-kinase Delta Inhibitor Nemiralisib

Bream, Robert N.,Clark, Hugh,Edney, Dean,Harsanyi, Antal,Hayler, John,Ironmonger, Alan,Mc Cleary, Nadine,Phillips, Natalie,Priestley, Catherine,Roberts, Alastair,Rushworth, Philip,Szeto, Peter,Webb, Michael R.,Wheelhouse, Katherine

, p. 529 - 540 (2021/03/01)

This paper describes the development of an improved and scalable method for the manufacture of nemiralisib, a phosphatidylinositol-3-kinase delta inhibitor. Incorporation of three consecutive catalytic reactions, including a palladium-catalyzed C-H functionalization and an iridium-catalyzed borylation, significantly simplified and shortened the synthetic sequence. The revised route was successfully implemented in a pilot plant on a multikilogram scale to deliver >100 kg of product.

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