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112259-66-2

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112259-66-2 Usage

Chemical Properties

White to off white powder

Check Digit Verification of cas no

The CAS Registry Mumber 112259-66-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,2,2,5 and 9 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 112259-66:
(8*1)+(7*1)+(6*2)+(5*2)+(4*5)+(3*9)+(2*6)+(1*6)=102
102 % 10 = 2
So 112259-66-2 is a valid CAS Registry Number.
InChI:InChI=1/C10H17NO4/c11-8(10(13)14)6-9(12)15-7-4-2-1-3-5-7/h7-8H,1-6,11H2,(H,13,14)/t8-/m0/s1

112259-66-2 Well-known Company Product Price

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  • Alfa Aesar

  • (H63707)  L-Aspartic acid 4-cyclohexyl ester, 95%   

  • 112259-66-2

  • 5g

  • 294.0CNY

  • Detail
  • Alfa Aesar

  • (H63707)  L-Aspartic acid 4-cyclohexyl ester, 95%   

  • 112259-66-2

  • 25g

  • 1176.0CNY

  • Detail
  • Alfa Aesar

  • (H63707)  L-Aspartic acid 4-cyclohexyl ester, 95%   

  • 112259-66-2

  • 100g

  • 4704.0CNY

  • Detail

112259-66-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name L-Aspartic acid 4-cyclohexyl ester

1.2 Other means of identification

Product number -
Other names L-Aspartic acid B-cyclohexyl 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:112259-66-2 SDS

112259-66-2Relevant articles and documents

An improved method for the preparation of ω-cyclohexyl esters of aspartic and glutamic acid

Toth,Penke

, p. 361 - 362 (1992)

An improved synthesis of β-cyclohexyl L-aspartate and γ-cyclohexyl L-glutamate and its N-tert-butoxycarbonyl (Boc) derivatives is described.

Cholesterol seco-sterol-induced aggregation of methylated amyloid-β peptides - Insights into aldehyde-initiated fibrillization of amyloid-β

Scheinost, Johanna C.,Wang, Hong,Boldt, Grant E.,Offer, John,Wentworth Jr., Paul

, p. 3919 - 3922 (2008/12/23)

(Chemical Equation Presented) Hot spot on amyloid-β? Atheronal-B-induced aggregation of amyloid-β (Aβ) involves a site-specific adduction of the aldehyde to the ε-amino group of Lys 16, suggesting that Lys 16 is a hot spot for atheronal-induced fibrilliza

Manipulation of Enzymatic Regioselectivity by Structural Modification of Substrates

Wu, Shih-Hsiung,Lo, Lee-Chiang,Chen, Shui-Tein,Wang, Kung-Tsung

, p. 4220 - 4222 (2007/10/02)

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