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193885-58-4

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193885-58-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 193885-58-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,9,3,8,8 and 5 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 193885-58:
(8*1)+(7*9)+(6*3)+(5*8)+(4*8)+(3*5)+(2*5)+(1*8)=194
194 % 10 = 4
So 193885-58-4 is a valid CAS Registry Number.

193885-58-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-[(2-chloroacetyl)amino]hexadecanoic acid

1.2 Other means of identification

Product number -
Other names Hexadecanoic acid,2-[(chloroacetyl)amino]

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:193885-58-4 SDS

193885-58-4Downstream Products

193885-58-4Relevant articles and documents

Novel aliphatic compounds, process for their preparation and their usage

-

Page/Page column 12, (2010/02/05)

The present invention provides an aliphatic compound represented by the following formula (I) or pharmacologically acceptable salts thereof: where n denotes an integer of 1 to 11, and 1 denotes an integer of 1 to 16, the aliphatic compound being an optical isomer of the (2R,3S,2′S) configuration when the 8-position thereof is a double bond, or an optical isomer of the (2S,3R,2′RS) configuration when the 8-position is a single bond; methods for producing the compound or pharmacologically acceptable salts thereof; and uses of the compound in the treatment of cardiovascular diseases (e.g. arteriosclerosis, cardiac diseases), cancer, rheumatism, diabetic retinopathy, and respiratory diseases.

ENZYMATIC FORMATION OF (2R)-HYDROXY- AND 2-OXO-HEXADECANOIC ACID IN ULVA PERTUSA AND PORPHYRA SP.

Kajiwara, Tadahiko,Kashibe, Masanori,Matsui, Kenji,Hatanaka, Akikazu

, p. 193 - 195 (2007/10/02)

(2R)-Hydroxy-hexadecanoic acid and 2-oxo-hexadecanoic acid have been isolated for the first time from marine algae (Ulva pertusa and Porphyra sp.).The two acids were shown to be formed enzymatically from palmitic acid (16:0) using palmitic acid.

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