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Benzenesulfonic acid, (iminophenoxymethyl)azanyl ester, also known as 4-(phenylsulfonyl)phenyl azane, is a chemical compound with the molecular formula C12H11NO3S. It is a derivative of benzenesulfonic acid, featuring an iminophenoxymethyl group attached to the azanyl (NH2) functional group. Benzenesulfonic acid,(iminophenoxymethyl)azanyl ester is characterized by its aromatic structure, with a benzene ring bearing a sulfonic acid group at the para position and an iminophenoxymethyl azane group at the ortho position. It is a white crystalline solid and is soluble in water. This chemical is primarily used in the synthesis of pharmaceuticals and other organic compounds due to its unique reactivity and functional groups. It is important to handle Benzenesulfonic acid,(iminophenoxymethyl)azanyl ester with care, as it may have potential health and environmental hazards.

3170-96-5

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3170-96-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3170-96-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,1,7 and 0 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 3170-96:
(6*3)+(5*1)+(4*7)+(3*0)+(2*9)+(1*6)=75
75 % 10 = 5
So 3170-96-5 is a valid CAS Registry Number.

3170-96-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name [(E)-[amino(phenoxy)methylidene]amino] benzenesulfonate

1.2 Other means of identification

Product number -
Other names N-benzenesulfonyloxy-O-phenylisourea

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:3170-96-5 SDS

3170-96-5Relevant academic research and scientific papers

Interaction of aryloxychlorocarbenes with acetylenedicarboxylate: Novel formation of polyfunctional butadienes and 8-oxatricyclo[3.2.1.0 2.4]oct-6-enes

Cheng, Ying,Zhu, Qing,Li, Quan Song,Meth-Cohn, Otto

, p. 4840 - 4846 (2007/10/03)

The interaction of aryloxychlorocarbenes with dialkyl acetylenedicarboxylates has been examined. Thermolyses of 3-aryloxy-3- chlorodiazirines in the presence of acetylenedicarboxylate resulted in the formation of unexpected polyfunctional 1,3-butadienes and 8-oxatricyclo[3.2.1. 02.4]oct-6-enes or of 2-aryoxycarbonylmaleates dependent upon reaction conditions. This work confirmed the nucleophilicity of aryloxychlorocarbenes and underlined their synthetic potential.

Phenoxychlorocarbene, a Second Ambiphile

Moss, Robert A.,Perez, Leon A.,Wlostowska, Joanna,Guo, Wenjeng,Krogh-Jespersen, Karsten

, p. 4177 - 4180 (2007/10/02)

Phenoxychlorocarbene (PhOCCl) was generated by thermolysis (25 deg C) of 3-chloro-3-phenoxydiazirine and added to six alkenes, affording the corresponding cyclopropanes.The substrates and (relative) reactivities were tetramethylethylene (3.0), isobutene (

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