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121933-59-3

(4-METHYL-4H-THIENO[3,2-B]PYRROL-5-YL)METHANOL, also known as AM-1248, is a synthetic cannabinoid that acts as a potent agonist for the cannabinoid receptors CB1 and CB2. It is an analog of JWH-018, a popular synthetic cannabinoid that was previously used in recreational drug blends. AM-1248 is known for its psychoactive effects, which can include feelings of euphoria, relaxation, and altered sensory perception.
Used in Recreational Drug Industry:
(4-METHYL-4H-THIENO[3,2-B]PYRROL-5-YL)METHANOL is used as a recreational drug for its psychoactive effects, which can include feelings of euphoria, relaxation, and altered sensory perception. However, it is important to note that these substances can have dangerous and potentially harmful effects on the body, and have been regulated and banned in many countries.
Used in Pharmaceutical Research:
(4-METHYL-4H-THIENO[3,2-B]PYRROL-5-YL)METHANOL is used as a research compound for studying the effects and mechanisms of action of synthetic cannabinoids on the cannabinoid receptors CB1 and CB2. Its higher affinity for these receptors compared to natural cannabinoids makes it a valuable tool for understanding the potential therapeutic applications of cannabinoids.

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  • 121933-59-3 Structure

  • Basic information

    1. Product Name: (4-METHYL-4H-THIENO[3,2-B]PYRROL-5-YL)METHANOL
    2. Synonyms: (4-METHYL-4H-THIENO[3,2-B]PYRROL-5-YL)METHANOL
    3. CAS NO:121933-59-3
    4. Molecular Formula: C8H9NOS
    5. Molecular Weight: 167.23
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 121933-59-3.mol

  • Chemical Properties

    1. Melting Point: 103 °C
    2. Boiling Point: 344.8 °C at 760 mmHg
    3. Flash Point: 162.3 °C
    4. Appearance: /
    5. Density: 1.32 g/cm3
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: (4-METHYL-4H-THIENO[3,2-B]PYRROL-5-YL)METHANOL(CAS DataBase Reference)
    10. NIST Chemistry Reference: (4-METHYL-4H-THIENO[3,2-B]PYRROL-5-YL)METHANOL(121933-59-3)
    11. EPA Substance Registry System: (4-METHYL-4H-THIENO[3,2-B]PYRROL-5-YL)METHANOL(121933-59-3)

  • Safety Data

    1. Hazard Codes: T
    2. Statements: 25
    3. Safety Statements: 45
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 121933-59-3(Hazardous Substances Data)

121933-59-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 121933-59-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,1,9,3 and 3 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 121933-59:
(8*1)+(7*2)+(6*1)+(5*9)+(4*3)+(3*3)+(2*5)+(1*9)=113
113 % 10 = 3
So 121933-59-3 is a valid CAS Registry Number.

121933-59-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name (4-methylthieno[3,2-b]pyrrol-5-yl)methanol

1.2 Other means of identification

Product number -
Other names 4H-Thieno[3,2-b]pyrrole-5-methanol,4-methyl

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:121933-59-3 SDS

121933-59-3Relevant articles and documents

A SYNTHESIS OF 4,7-DIHYDRO-1H-DIPYRROLOPYRROLE AND 4,7-DIHYDRO-4H-THIENOPYRROLOPYRROLE SYSTEMS

Aratani, Tadatoshi,Yoshihara, Hiroshi,Suzukamo, Gohfu

, p. 1655 - 1656 (1989)

The titled two systems (3 and 6), both new members of linearly fused heteroaromatics, were prepared using pyrrolo-annulation reaction: condensation of an aromatic aldehyde with azidoacetate followed by thermolysis of the resulting azidoacrylate.

Discovery of Reversible Inhibitors of KDM1A Efficacious in Acute Myeloid Leukemia Models

Romussi, Alessia,Cappa, Anna,Vianello, Paola,Brambillasca, Silvia,Cera, Maria Rosaria,Dal Zuffo, Roberto,Fagà, Giovanni,Fattori, Raimondo,Moretti, Loris,Trifirò, Paolo,Villa, Manuela,Vultaggio, Stefania,Cecatiello, Valentina,Pasqualato, Sebastiano,Dondio, Giulio,So, Chi Wai Eric,Minucci, Saverio,Sartori, Luca,Varasi, Mario,Mercurio, Ciro

, p. 754 - 759 (2020)

Lysine-specific demethylase 1 (LSD1 or KDM1A) is a FAD-dependent enzyme that acts as a transcription corepressor or coactivator by regulating the methylation status of histone H3 lysines K4 and K9, respectively. KDM1A represents an attractive target for c

Self-condensation of N-substituted (4H-thieno[3,2-b]-pyrrol-5-yl)methanols into bis(thienopyrrolyl)methanes

Torosyan, Seda A.,Zagitov, Vadim V.,Gimalova, Fanuza A.,Biglova, Raisa Z.,Miftakhov, Mansur S.

, p. 192 - 194 (2018)

N-Substituted (4H-thieno[3,2-b]pyrrol-5-yl)methanols were obtained by alkylation of methyl 4H-thieno[3,2-b]pyrrole-5-carboxylate followed by reduction with LiAlH4. These compounds on contact with Amberlyst 15 (H-form) in CH2Cl2

Synthesis of N-Substituted Methyl 4H-Thieno[3,2-b]pyrrole-5-carboxylates

Torosyan,Gimalova,Zagitov,Erastov,Miftakhov

, p. 912 - 917 (2018/07/31)

The alkylation of methyl 4H-thieno[3,2-b]pyrrole-5-carboxylate with methyl iodide and allyl, propargyl, and benzyl bromides in the presence of sodium hydride in THF afforded the corresponding N-substituted derivatives. Some reactions of the alkylation products were studied.

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