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63321-54-0

63321-54-0

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63321-54-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 63321-54-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,3,3,2 and 1 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 63321-54:
(7*6)+(6*3)+(5*3)+(4*2)+(3*1)+(2*5)+(1*4)=100
100 % 10 = 0
So 63321-54-0 is a valid CAS Registry Number.
InChI:InChI=1/C15H22N2O4/c1-2-3-4-5-6-7-12-16-15(18)21-14-10-8-13(9-11-14)17(19)20/h8-11H,2-7,12H2,1H3,(H,16,18)

63321-54-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name (4-nitrophenyl) N-octylcarbamate

1.2 Other means of identification

Product number -
Other names 4-nitrophenyl-N-n-octyl carbamate

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:63321-54-0 SDS

63321-54-0Downstream Products

63321-54-0Relevant articles and documents

Structure-reactivity relationships as probes for the inhibition mechanism of cholesterol esterase by aryl carbamates. I. Steady-state kinetics

Lin, Gialih,Lai, Cheng-Yue,Liao, Wei-Cheng,Kuo, Bing-Hong,Lu, Chun-Ping

, p. 489 - 500 (2007/10/03)

For substituted phenyl-N-butyl carbamates (1) and 4-nitrophenyl-N-substituted carbamates (2), linear relationships between values of NH proton chemical shift (δNH), pKa, and logk[OH] and Hammett substituent constant (σ) or Taft subst

Linear free energy relationships of the inhibition of pancreatic cholesterol esterase by 4-nitrophenyl-N-alkylcarbamate

Lin, Gialih,Lai, Cheng-Yue

, p. 193 - 196 (2007/10/02)

4-Nitrophenyl-N-alkylcarbamates (1) as active site-directed irreversible inhibitors of pancreatic cholesterol esterase are investigated for values of the dissociation constant (K(i)), the carbamylation constant (k2), and the bimolecular rate co

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