65911-47-9

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Basic information

Product Name: Benzoic acid, 2-(aminocarbonyl)-4-nitro-
Synonyms:
CAS NO:65911-47-9
Molecular Formula: C8H6N2O5
Molecular Weight: 210.146
EINECS: N/A
Product Categories: N/A
Mol File: 65911-47-9.mol
Article Data: 2

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: Benzoic acid, 2-(aminocarbonyl)-4-nitro-(CAS DataBase Reference)
NIST Chemistry Reference: Benzoic acid, 2-(aminocarbonyl)-4-nitro-(65911-47-9)
EPA Substance Registry System: Benzoic acid, 2-(aminocarbonyl)-4-nitro-(65911-47-9)

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: 65911-47-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 65911-47-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,5,9,1 and 1 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 65911-47:
(7*6)+(6*5)+(5*9)+(4*1)+(3*1)+(2*4)+(1*7)=139
139 % 10 = 9
So 65911-47-9 is a valid CAS Registry Number.

65911-47-9SDS

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	2-carbamoyl-4-nitrobenzoic acid

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).

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65911-47-9Relevant articles and documents

Phthalimidomethyl as a drug pro-moiety. Probing its reactivity

Iley, Jim,Calheiros, Teresa,Moreira, Rui

, p. 955 - 958 (1998)

Phthalimidomethyl derivatives 1, encompassing a wide range of leaving group abilities, are rapidly hydrolysed to the corresponding phthalamic acid via rate-determining attack at the phthalimide carbonyl group.

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