Cas 260392-41-4,Hydrazinecarboxylic acid, 2-[(1S,2R)-2-(acetyloxy)cyclohexyl]-2-methyl-, 1,1-dimethylethyl ester

260392-41-4

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Basic information

Product Name: Hydrazinecarboxylic acid, 2-[(1S,2R)-2-(acetyloxy)cyclohexyl]-2-methyl-, 1,1-dimethylethyl ester
Synonyms:
CAS NO:260392-41-4
Molecular Formula: C14H26N2O4
Molecular Weight: 286.371
EINECS: N/A
Product Categories: N/A
Mol File: 260392-41-4.mol

Chemical Properties

Melting Point: N/A
Boiling Point: N/A
Flash Point: N/A
Appearance: N/A
Density: N/A
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: Hydrazinecarboxylic acid, 2-[(1S,2R)-2-(acetyloxy)cyclohexyl]-2-methyl-, 1,1-dimethylethyl ester(CAS DataBase Reference)
NIST Chemistry Reference: Hydrazinecarboxylic acid, 2-[(1S,2R)-2-(acetyloxy)cyclohexyl]-2-methyl-, 1,1-dimethylethyl ester(260392-41-4)
EPA Substance Registry System: Hydrazinecarboxylic acid, 2-[(1S,2R)-2-(acetyloxy)cyclohexyl]-2-methyl-, 1,1-dimethylethyl ester(260392-41-4)

Safety Data

Hazard Codes: N/A
Statements: N/A
Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 260392-41-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 260392-41-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,6,0,3,9 and 2 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 260392-41:
(8*2)+(7*6)+(6*0)+(5*3)+(4*9)+(3*2)+(2*4)+(1*1)=124
124 % 10 = 4
So 260392-41-4 is a valid CAS Registry Number.

260392-41-4Upstream product

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260392-41-4Relevant academic research and scientific papers

Enzymatic resolution of (±)-2-(N(β)-t-butoxycarbonyl-N(α)- methylhydrazino)cycloalkanols

Forro, Eniko,Szakonyi, Zsolt,Fueloep, Ferenc

, p. 4619 - 4626 (2007/10/03)

Racemates of cis- and trans-2-(N(β)-t-butoxycarbonyl-N(α)- methylhydrazino)cyclopentanols and -cyclohexanols 1-4 were resolved through lipase PS- or Novozym 435-catalysed asymmetric acylation of the secondary OH group at the (R)-stereogenic centre. High e

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