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130309-46-5

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130309-46-5 Usage

Uses

4-(Boc-amino)cyclohexanecarboxylic acid is used as pharmaceutical intermediate.

Check Digit Verification of cas no

The CAS Registry Mumber 130309-46-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,0,3,0 and 9 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 130309-46:
(8*1)+(7*3)+(6*0)+(5*3)+(4*0)+(3*9)+(2*4)+(1*6)=85
85 % 10 = 5
So 130309-46-5 is a valid CAS Registry Number.
InChI:InChI=1/C12H21NO4/c1-12(2,3)17-11(16)13-9-6-4-8(5-7-9)10(14)15/h8-9H,4-7H2,1-3H3,(H,13,16)(H,14,15)

130309-46-5 Well-known Company Product Price

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  • Alfa Aesar

  • (H52573)  4-(Boc-amino)cyclohexanecarboxylic acid, 97%   

  • 130309-46-5

  • 250mg

  • 425.0CNY

  • Detail
  • Alfa Aesar

  • (H52573)  4-(Boc-amino)cyclohexanecarboxylic acid, 97%   

  • 130309-46-5

  • 1g

  • 1274.0CNY

  • Detail
  • Alfa Aesar

  • (H52573)  4-(Boc-amino)cyclohexanecarboxylic acid, 97%   

  • 130309-46-5

  • 5g

  • 5096.0CNY

  • Detail

130309-46-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-(BOC-AMINO)CYCLOHEXANECARBOXYLIC ACID

1.2 Other means of identification

Product number -
Other names Trans-4-Boc-cyclohexanecarboxylic 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:130309-46-5 SDS

130309-46-5Relevant articles and documents

Rigid aromatic linking moiety in cationic lipids for enhanced gene transfection efficiency

Wang, Bing,Zhao, Rui-Mo,Zhang, Ji,Liu, Yan-Hong,Huang, Zheng,Yu, Qing-Ying,Yu, Xiao-Qi

, p. 585 - 595 (2017)

Although numerous cationic lipids have been developed as non-viral gene vectors, the structure-activity relationship (SAR) of these materials remains unclear and needs further investigation. In this work, a series of lysine-derived cationic lipids contain

Preparation method of trans 4 - (tert-butyloxycarbonylamino) cyclohexanecarboxylic acid and intermediate thereof

-

, (2021/09/21)

The invention provides a preparation method of trans 4 - (tert-butyloxycarbonylamino) cyclohexanecarboxylic acid and an intermediate thereof. The preparation method is characterized by comprising the following steps of 4 - oxocyclohexane carboxylic ester and chiral ligand reagent tert-butyl sulfinamide as a raw material, reducing amination to obtain trans -4 -tert-butyl sulfinyl sulfenamide cyclohexane carboxylic acid ester by virtue of chiral ligand reagent tert-butyl sulfinamide and 4 - 95% -oxocyclohexane carboxylic ester, and is stable in basic conditions and easy to leave under an acidic condition. Reaction conditions are mild, operation is simple and convenient, yield is high, and industrial production is easy.

Compound serving as protein kinase inhibitor and application of compound

-

Paragraph 0330-0333, (2021/04/07)

The invention discloses a compound used as a protein kinase inhibitor and application of the compound, the compound has an obvious inhibition effect on protein kinase activity, can be used as a BTK inhibitor for preparing medicines for treating BTK-mediated diseases such as malignant tumors, autoimmune diseases and the like, and has wide application prospect.

Generation of highly potent DYRK1A-dependent inducers of human β-Cell replication via Multi-Dimensional compound optimization

Allegretti, Paul A.,Horton, Timothy M.,Abdolazimi, Yassan,Moeller, Hannah P.,Yeh, Benjamin,Caffet, Matthew,Michel, Guillermina,Smith, Mark,Annes, Justin P.

supporting information, (2019/12/09)

Small molecule stimulation of β-cell regeneration has emerged as a promising therapeutic strategy for diabetes. Although chemical inhibition of dual specificity tyrosine-phosphorylation-regulated kinase 1A (DYRK1A) is sufficient to enhance β-cell replicat

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