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Pyrrolo[2,3-b]indole-1(2H)-carboxylic acid, 3,3a,8,8a-tetrahydro-3a-hydroxy-, methyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

58635-36-2

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58635-36-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 58635-36-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,8,6,3 and 5 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 58635-36:
(7*5)+(6*8)+(5*6)+(4*3)+(3*5)+(2*3)+(1*6)=152
152 % 10 = 2
So 58635-36-2 is a valid CAS Registry Number.

58635-36-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name methyl 1,2,3,3a,8,8a-hexahydro-3a-hydroxypyrrolo[2,3-b]indole-1-carboxylate

1.2 Other means of identification

Product number -
Other names 3a-hydroxy-3,3a,8,8a-tetrahydro-2H-pyrrolo[2,3-b]indole-1-carboxylic acid methyl ester

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:58635-36-2 SDS

58635-36-2Relevant academic research and scientific papers

Nucleophilic substitution reaction on the nitrogen of indole nucleus: A novel synthesis of 1-aryltryptamines

Hayashi, Toshikatsu,Peng, Wu,Nakai, Yu Ya,Yamada, Koji,Somei, Masanori

, p. 421 - 424 (2007/10/03)

1-Hydroxytryptamine derivatives undergo nucleophilic substitution reaction on the indole nitrogen (Na) as a general reaction by the treatment with acid, providing a novel synthetic method for 1-aryltryptamines. Depending on the structures of nucleophiles,

DYE-SENSITIZED PHOTOOXYGENATION OF TRYPTOPHAN: 3a-HYDROPEROXYPYRROLOINDOLE AS A LABILE PRECURSOR OF FORMYLKYNURENINE

Nakagava, Masako,Kato, Shiro,Kataoka, Shigehiro,Kodato, Shinichi,Watanabe, Hideyuki,et al.

, p. 1013 - 1026 (2007/10/02)

The isolation, structure determination, and reactivity of the tricyclic labile hydroperoxides 10 and 2 obtained by dye-sensitized photooxygenation of L-, D-, and DL-tryptophan and Nb-methoxycarbonyltryptophan ester are reported.The tricyclic hydroperoxide 10, under apprpopiate conditions, was easily convertible to formylkynurenine.Plausible mechanisms for these transformations are discussed.Keywords-tryptophan and its derivatives; dye-sensitized photooxygenation; formylkynurenine; hydroperoxypyrroloindoles; 3-hydroperoxyindolenines; 1,3-benzoxazines; CD spectra; rearrangement; ring-chain tautomerism; biological oxidation

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