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837392-67-3

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  • Cas no.837392-67-3 98% tert-butyl 5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)indoline-1-carboxylate

    Cas No: 837392-67-3

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  • 100kg+ Metric Ton/Day

  • Win-Win chemical Co.Ltd
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  • 837392-67-3 1H-Indole-1-carboxylic acid, 2,3-dihydro-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-, 1,1-dimethylethyl ester

    Cas No: 837392-67-3

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  • Hangzhou Fandachem Co.,Ltd
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  • 1H-Indole-1-carboxylic acid, 2,3-dihydro-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-, 1,1-dimethylethyl ester

    Cas No: 837392-67-3

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837392-67-3 Usage

Uses

1-Boc-indoline-5-boronic acid pinacol ester is used as disinfector, tanning agent.

Check Digit Verification of cas no

The CAS Registry Mumber 837392-67-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,3,7,3,9 and 2 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 837392-67:
(8*8)+(7*3)+(6*7)+(5*3)+(4*9)+(3*2)+(2*6)+(1*7)=203
203 % 10 = 3
So 837392-67-3 is a valid CAS Registry Number.

837392-67-3 Well-known Company Product Price

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  • Alfa Aesar

  • (H59436)  1-Boc-indoline-5-boronic acid pinacol ester, 97%   

  • 837392-67-3

  • 250mg

  • 819.0CNY

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  • Alfa Aesar

  • (H59436)  1-Boc-indoline-5-boronic acid pinacol ester, 97%   

  • 837392-67-3

  • 1g

  • 2621.0CNY

  • Detail

837392-67-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name tert-butyl 5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-2,3-dihydroindole-1-carboxylate

1.2 Other means of identification

Product number -
Other names 1-Boc-indoline-5-boronic acid pinacol ester

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:837392-67-3 SDS

837392-67-3Downstream Products

837392-67-3Relevant articles and documents

PERK INHIBITING INDOLINYL COMPOUNDS

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Paragraph 0142; 0146; 0147, (2021/03/05)

Provided herein are compounds of formula (I), compositions, and methods useful for inhibiting PERK and for treating related conditions diseases, and disorders, wherein Q is selected from (Ia), (Ib) ou (Ic).

4-aminopyrrolopyrimidine derivative and preparation method and application thereof

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Paragraph 0137-0138; 0142; 0153-0154, (2020/05/14)

The invention relates to a 4-aminopyrrolopyrimidine derivative and a preparation method and application thereof, and belongs to the field of medicines. The invention provides a compound shown as a formula I or pharmaceutically acceptable salt thereof. The

Identification of 5-(2,3-Dihydro-1 H-indol-5-yl)-7 H-pyrrolo[2,3- d]pyrimidin-4-amine Derivatives as a New Class of Receptor-Interacting Protein Kinase 1 (RIPK1) Inhibitors, Which Showed Potent Activity in a Tumor Metastasis Model

Li, Yueshan,Xiong, Yu,Zhang, Guo,Zhang, Liting,Yang, Wei,Yang, Jiao,Huang, Luyi,Qiao, Zeen,Miao, Zhuang,Lin, Guifeng,Sun, Qiu,Niu, Ting,Chen, Lijuan,Niu, Dawen,Li, Linli,Yang, Shengyong

, p. 11398 - 11414 (2019/01/08)

We herein report the structural optimization and structure-activity relationship studies of 5-(2,3-dihydro-1H-indol-5-yl)-7H-pyrrolo[2,3-d]pyrimidin-4-amine derivatives as a new class of receptor-interacting protein kinase 1 (RIPK1) inhibitors. Among all obtained RIPK1 inhibitors, 1-(5-{4-amino-7-ethyl-7H-pyrrolo[2,3-d]pyrimidin-5-yl}-2,3-dihydro-1H-indol-1-yl)-2-[3-(trifluoromethoxy)phenyl]ethan-1-one (22b) is the most active one. This compound potently inhibited RIPK1 with a binding affinity (KD) of 0.004 μM and an enzymatic IC50 value of 0.011 μM and also showed good kinase selectivity. It could efficiently protect cells from necroptosis and attenuate the necrotic cell death of vascular endothelial cells induced by tumor cells both in vitro and in vivo. Importantly, compound 22b exhibited excellent antimetastasis activity in the experimental B16 melanoma lung metastasis model. It also displayed favorable pharmacokinetic properties. Collectively, 22b could be a promising agent for preventing tumor metastasis.

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