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115730-36-4

1,3-Cyclohexanedicarboxylicacid,1-amino-,(1R-trans)-(9CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 115730-36-4 Structure

  • Basic information

    1. Product Name: 1,3-Cyclohexanedicarboxylicacid,1-amino-,(1R-trans)-(9CI)
    2. Synonyms: 1,3-Cyclohexanedicarboxylicacid,1-amino-,(1R-trans)-(9CI)
    3. CAS NO:115730-36-4
    4. Molecular Formula: C8H13NO4
    5. Molecular Weight: 187.19
    6. EINECS: N/A
    7. Product Categories: AMINOACID
    8. Mol File: 115730-36-4.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 363.1±42.0 °C(Predicted)
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: 1.366±0.06 g/cm3(Predicted)
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. PKA: 2.74±0.50(Predicted)
    10. CAS DataBase Reference: 1,3-Cyclohexanedicarboxylicacid,1-amino-,(1R-trans)-(9CI)(CAS DataBase Reference)
    11. NIST Chemistry Reference: 1,3-Cyclohexanedicarboxylicacid,1-amino-,(1R-trans)-(9CI)(115730-36-4)
    12. EPA Substance Registry System: 1,3-Cyclohexanedicarboxylicacid,1-amino-,(1R-trans)-(9CI)(115730-36-4)

  • 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: 115730-36-4(Hazardous Substances Data)

115730-36-4 Usage

Explanation

The molecular formula represents the number of atoms of each element present in a molecule of the compound.
2. Derivative of cyclohexane

Explanation

The compound is derived from cyclohexane, which is a six-carbon ring structure with no double bonds.
3. Carboxylic acid functional groups

Explanation

The compound contains two carboxylic acid groups (-COOH), which are acidic and can form hydrogen bonds.
4. Amino functional group

Explanation

The compound has one amino group (-NH2), which is a basic functional group and can form hydrogen bonds.

Explanation

The compound has a specific stereochemistry, with one of the carboxylic acid groups in a trans configuration. This means that the two functional groups are on opposite sides of the cyclohexane ring.

Explanation

The compound may have various applications in different industries due to its unique structure and functional groups.
7. Building block for organic synthesis

Explanation

The compound's structure and functional groups make it a potential building block for the synthesis of various organic molecules.
8. Reactivity and selectivity in chemical reactions

Explanation

The compound's stereochemistry may impart specific reactivity or selectivity in certain chemical reactions, making it useful for targeted synthesis.
9. Further research and development

Explanation

Additional research and development may uncover more uses and potential benefits of this compound, expanding its applications and importance in various fields.

Stereochemistry

1R-trans

Potential applications

Pharmaceuticals, polymers, and industrial processes

Check Digit Verification of cas no

The CAS Registry Mumber 115730-36-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,5,7,3 and 0 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 115730-36:
(8*1)+(7*1)+(6*5)+(5*7)+(4*3)+(3*0)+(2*3)+(1*6)=104
104 % 10 = 4
So 115730-36-4 is a valid CAS Registry Number.

115730-36-4SDS

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 1,3-Cyclohexanedicarboxylicacid,1-amino-,(1R-trans)-(9CI)

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:115730-36-4 SDS

115730-36-4Relevant articles and documents

Resolution and regioselective protection of glutamic acid analogues. I- Resolution of diastereomeric α-boroxazolidone derivatives

Acher,Azerad

, p. 731 - 744 (2007/10/02)

Diastereomeric α-boroxazolidone γ-phenylethylamide (or γ-phenylethanolamide) derivatives of 2-, 3- or 4-substituted glutamic acid analogues have been separated by silicagel chromatography, resulting, after deprotection, in a practical method for the resolution of most of these unnatural amino acids.

Synthesis and resolution of DHCGA, a new conformationally rigid 3,4-dehydroglutamic acid analogue

Trigalo, Francois,Acher, Francine,Azerad, Robert

, p. 5203 - 5212 (2007/10/02)

(±)-1-amino-2-cyclohexene-1,3-dicarboxylic acid (DHCGA),an unsaturated cyclic analogue of glutamic acid, was prepared from 3-carboxy-4-cyclohexenone by a Bucherer-Bergs reaction. Resolution was performed through coupling with L-leucine and separation of the resulting diastereoisomeric dipeptides. Spectral data, including optical rotation and circular dichroism of both enantiomers of DHCGA are reported.

CHEMOENZYMATIC SYNTHESIS OF CONFORMATIONALLY RIGID GLUTAMIC ACID ANALOGUES

Trigalo, F.,Buisson, D.,Azerad, R.

, p. 6109 - 6112 (2007/10/02)

All stereomers of cyclohexane cyclopentane-derived analogues of glutamic acid have been synthesized from the corresponding 3-keto-cycloalkyl carboxylic acid esters by a combination of microbial steps and standard chemical methods.

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